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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076938Generated: October 31, 2026

Benzyl mercaptan → HCID 25130204, compound

https://huagongshe.com/reaction/2076938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 67099447HCID 67099447—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25130204HCID 25130204—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of n-BuLi (2.5M in hexanes, 10 mL) was added slowly to a solution of benzyl mercaptan (3.6 mL, 40 mmol) in THF (40 mL) at 0° C. The resulting pale-yellow solution was stirred at 0° C. for 10 min prior to the introduction of (4R)-4-benzyl-3-({(1R,2R)-2-[(benzyloxy)methyl]-4,4-difluorocyclohexyl}carbonyl)-1,3-oxazolidin-2-one (8.52 g, 19.2 mmol) as a solution in THF (30 mL). After 10 min, a solution of LiAlH4 (1.0 M in THF, 22 mL) was slowly added to the reaction mixture with continued stirring at 0° C. for 45 min. Ice water was then slowly added to destroy excess hydride followed by 6M HCl (20 mL) to pH 1. The mixture was extracted with two portions of ethyl acetate and the combined organics were washed with saturated aqueous NaCl and dried over Na2SO4. Concentration in vacuo and flash chromatography of the residue on silica gel eluting with 45/55 ethyl acetate/hexanes afforded {(1R,2R)-2-[(benzyloxy)methyl]-4,4-difluorocyclohexyl}methanol as a thick, colorless syrup. 1H NMR (500 MHz, d6-acetone) δ 7.36 (4H, m), 7.34-7.28 (1H, m), 4.56-4.49 (2H, m), 3.67-3.53 (5H, m), 2.20-2.12 (1H, m), 2.09-2.02 (1H, m), 1.91-1.71 (4H, m), 1.58-1.50 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928091B2
Source datasetuspto-grants-2011_04
ORD IDord-efdf53af509f429b9226d0da34f40498
Source noteuspto-grants-2011_04