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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129312Generated: October 27, 2026

Diethyl Ether → 2,2-Di(benzylthiomethyl)pentanal

https://huagongshe.com/reaction/129312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium AcetateHCID 517045—
Reactant2,2-Di(benzylthiomethyl)pentan-1-olHCID 19373328—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product2,2-Di(benzylthiomethyl)pentanalHCID 19373415—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 2,2-di-(benzylthiomethyl)pentan-1-ol (1.0 g Example XI) in dry dichloromethane (10 ml) was added to a stirred suspension of pyridinium chlorochromate (1.5 g) and anhydrous sodium acetate (0.11 g) in dry dichloromethane (25 ml) at 0° C., under a current of nitrogen. The reaction mixture was allowed to warm to 20° C. and then stirred for 2 hours. Dry diethyl ether was added and the mixture stirred for 30 minutes. The ethereal extracts were decanted off and the residue was washed with further portions of diethyl ether. The combined ethereal extracts were dried over anhydrous magnesium sulphate and the solvent was removed in vacuo. The residue was purified by chromatography on a mixture of silica and charcoal, eluting with diethyl ether. 2,2-Di(benzylthiomethyl)pentanal was obtained as a pale yellow oil (0.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466710
Source datasetuspto-grants-1995_11
ORD IDord-6d1d7433fbd64c8d934a486f6715ca7b
Source noteuspto-grants-1995_11