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Record W1588790426 · doi:10.1002/047084289x.rn01655

[2-(Amino-κ<i>N</i>)ethanolato-κ<i>O</i>]diphenylboron

2014· reference-entry· he· W1588790426 on OpenAlexaff
Mark S. Taylor

Bibliographic record

VenueEncyclopedia of Reagents for Organic Synthesis · 2014
Typereference-entry
Languagehe
FieldChemistry
TopicCarbohydrate Chemistry and Synthesis
Canadian institutionsUniversity of Toronto
Fundersnot available
KeywordsChemistryEthanolamineOrganic chemistryHydrochlorideReagentMedicinal chemistryNuclear chemistry

Abstract

fetched live from OpenAlex

[15614-89-8] C14H16BNO (MW 225.10) InChI = 1S/C14H16BNO/c1-3-7-13(8-4-1)15(16-11-12-17-15)14-9-5-2-6-10-14/h1-10H,11-12,16H2 InChIKey = QKVRQZFQCGZLDA-UHFFFAOYSA-N (reagent for derivatization of flavonoids; inhibitor of Ca2+ channels; precursor to diphenylborinic acid; precatalyst for regioselective acylation, alkylation, sulfonylation, and glycosylation reactions) Alternate Names: 2-aminoethyl diphenylborinate; 2-APB; diphenylborinic acid 2-aminoethyl ester; Natural Product Reagent A. Physical Data: white crystalline solid, mp 189–190 °C. Solubility: soluble in acetone, DMSO, DMF, methanol, and THF. Preparative Methods: condensation of diphenylborinic acid or a diphenylborinate ester with ethanolamine. Diphenylborinic acid and esters thereof are generated by addition of phenylmagnesium halides to trialkyl borates. Several variants of the protocol have been reported. The ammonia complex of diphenylborinic acid isobutyl ester may be generated by addition of phenylmagnesium bromide to B(Oi-Bu)3, followed by hydrolysis and treatment with anhydrous NH3. Treatment of this complex with ethanolamine in toluene at reflux yields the crystalline ethanolamine ester.1 Addition of phenylmagnesium bromide to trimethoxyboroxine, quenching with aqueous HCl, and complexation with ethanolamine in water generates the diphenylborinate ester in 62% yield.2 A similar procedure employing phenylboroxine in place of trimethoxyboroxine has been reported.3 Aminoethyl diphenylborinate may also be prepared by treatment of triphenylborane with ethanolamine in refluxing benzene,4 or from sodium tetraphenylborate and ethanolamine hydrochloride.5 Purification: recrystallization (e.g., from ethanol/water). Handling, Storage, and Precautions: borinic acids are frequently isolated as their ethanolamine adducts because of the resistance of the latter to oxidation under ambient conditions, as well as their ease of purification by recrystallization. Aminoethyl diphenylborinate has been reported to be stable upon storage for up to 3 years on the bench top,6 although storage at −20 °C is recommended by certain suppliers. Hydrolysis of aminoethyl diphenylborinate to diphenylborinic acid is accomplished by treatment with aqueous acid.1, 6 The kinetics of this process have been studied in detail.7 Dissociation of the complex takes place within a few minutes in aqueous phosphate buffer at pH 7.0.8

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: none
GenreCandidate signal: Other · Consensus signal: none
Teacher disagreement score0.016
Threshold uncertainty score0.052

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0160.006

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.015
GPT teacher head0.236
Teacher spread0.221 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNot applicable
Domainnot available
GenreOther

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2014
Admission routes1
Has abstractyes

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