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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109391Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 15107107, compound

https://huagongshe.com/reaction/1109391

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,2-DimethoxypropaneHCID 6495—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 15107105HCID 15107105—
SolventDichloromethaneHCID 6344—
ProductHCID 15107107HCID 15107107—

Reaction Steps

983 mg of (3RS,4S)-4-(benzyloxycarbonyl)amino-5-cyclohexylpentene-3-ol was dissolved in 5 ml of dichloromethane, and 4 ml of 2,2-dimethoxypropane and 30 mg of dry p-toluenesulfonic acid were added thereto. The mixture was stirred at room temperature overnight. Then, 100 ml of ethyl acetate was added to the reaction mixture. The mixture was washed with a saturated sodium hydrogencarbonate aqueous solution and with a saturated sodium chloride aqueous solution. Then, the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by-silica gel column chromatography (n-hexane/ethyl acetate=20/1) to obtain 967 mg of (4S,5RS)-3-benzyloxycarbonyl-4-cyclohexylmethyl-5-ethenyl-2,2-dimethyloxazolidine as colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05319082
Source datasetuspto-grants-1994_06
ORD IDord-318e5504a346410b83e5e1001c9bae07
Source noteuspto-grants-1994_06