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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045125Generated: October 26, 2026

Tetrahydrofuran → 4-Chlorobenzhydrol, (S)-

https://huagongshe.com/reaction/1045125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMagnesiumHCID 5462224—
Reactant4-ChlorobenzenebromideHCID 86664079—
ReactantHCID 178418255HCID 178418255—
ReactantHCID 178478191HCID 178478191—
Product4-Chlorobenzhydrol, (S)-HCID 852995—

Reaction Steps

An operation was carried out in the same manner as in Example 14, except that 0.29 mL (0.375 mmol) of 4-chlorophenylmagnesium bromide (1.4 mol/L) prepared from magnesium and 4-chlorobenzene bromide was used instead of the anhydrous THF solution of phenylmagnesium bromide. Thus, (S)-4-chlorobenzhydrol was obtained. The conversion rate of the raw material was 96%, while the enantiomeric excess was 92% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563786B2
Source datasetuspto-grants-2013_10
ORD IDord-9e34341444364e5dadce0824d5b68431
Source noteuspto-grants-2013_10