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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258137Generated: October 26, 2026

Borane → HCID 178419237, compound

https://huagongshe.com/reaction/258137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant2-Pyrrolidinemethanol, alpha,alpha-diphenyl-, (S)-HCID 2724899—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventTolueneHCID 1140—
ProductHCID 178419237HCID 178419237—

Reaction Conditions

Temperature20 °C

Reaction Steps

A 250-mL three-necked flask fitted with a mechanical stirrer, nitrogen inlet tube, and teflon coated thermocouple probe, was charged with a solution of the free base product of Example 1 Step B (20.7 g, 81.7 mmol) in dry toluene (100 mL). To the stirred solution at 20° C. was added borane-dimethyl sulfide (10M, 10.0 mL, 100 mmol) over 5 minutes via syringe. The borane reacted immediately in an exothermic reaction (raising the internal temperature from 20° C. to 32° C.) forming a thick white precipitate. With continued stirring, the mixture was allowed to cool to room temperature (20° C.) over a 1 hour period. The mixture was filtered, and the product cake washed with dry toluene (25 mL). The product was dried in vacuo (20° C., 0.01 mBar) to constant weight. Yield 15.7 g (72%) of a white crystal line solid. m.p. 130°-132° C. (dec). 1H NMR (CDCl3 ) δ7.7-7.1 (m, 10 H, Ar-H), 5.15 (s, 1 H, --OH), 4.5 (br, 1 H, --NH), 4.2 (m, 1 H, C2-H), 3.25 (m, 2 H, C5-H2), 2.6 (m, 1 H, C4- H), 2.3 (m, 1 H, C4-H), 1.85 (m, 1 H, C3-H), 1.6 (m, 1 H, C3-H), 2.1-0.7 (br, 3 H, BH3). 13C NMR (CDCl3) δ145.8, 144.5 (C1', C1"), 129.1, 128.2 (C3', C5', C3", C5"), 127.4, 127.0 (C4', C4"), 125.2, 125.1 (C2', C6', C2", C6"), 76.5 (Cα), 69.6 (C2), 55.6 (C 5), 20.6 (C4), 19.9 (C3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264585
Source datasetuspto-grants-1993_11
ORD IDord-969b93af375048c4b3dc8543aaf96b43
Source noteuspto-grants-1993_11