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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045129Generated: October 27, 2026

Tetrahydrofuran → (R)-Phenyl(p-tolyl)methanol

https://huagongshe.com/reaction/1045129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 178418255HCID 178418255—
ReactantHCID 178420449HCID 178420449—
Product(R)-Phenyl(p-tolyl)methanolHCID 7003729—

Reaction Steps

An operation was carried out in the same manner as in Example 1, except that 0.40 mL (0.40 mmol) of an anhydrous THF solution (1.0 mol/L) of phenylmagnesium bromide was used instead of the anhydrous 1,4-dioxane solution of diphenylmagnesium. Thus, (R)-4-methylbenzhydrol was obtained. The conversion rate of the raw material was 98%, while the enantiomeric excess was 39% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563786B2
Source datasetuspto-grants-2013_10
ORD IDord-b06b146eaa6f4ae1b3da036c8094e0b9
Source noteuspto-grants-2013_10