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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004495Generated: October 30, 2026

Dimethyl Sulfide → (R,E)-4-phenylthio-3-buten-2-ol

https://huagongshe.com/reaction/1004495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantAmmonium ChlorideHCID 25517—
Reactant(3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaboroleHCID 2734713—
Reactant4-(Phenylsulfanyl)but-3-en-2-oneHCID 6269152—
SolventTolueneHCID 1140—
Product(R,E)-4-phenylthio-3-buten-2-olHCID 11019465—

Reaction Steps

(E)-4-phenylthio-3-buten-2-one (178 mg, 1.0 mmol), (S)-3,3-diphenyl-1-methyltetrahydro-1H,3H-pyrrolo[1,2-c] [1,3,2] oxazaborol (28 mg, 0.1 mmol) and MS4A (Nacalai Tesque Inc., 500 mg) were dried by a vacuum pump, followed by substituting with an argon gas. Dry toluene (5 ml) and dimethylsulfide (3.0 mmol) were added thereto and, after ice cooling, a solution of borane dimethylsulfide complex in toluene (1.07M, 0.65 ml, 0.7 mmol) was dropwise added. After stirring for two hours, an aqueous saturated ammonium chloride solution was added, followed by filtering through a cotton plug. The filtrate was washed with ethyl acetate and, after separating an aqueous layer, the organic layer was washed with 2NHCl, water, an aqueous saturated sodium hydrogen carbonate solution, water and saturated brine. After drying with anhydrous magnesium sulfate, the extract containing the titled compound as a main component was obtained by concentrating under a reduced pressure. The NMR chemical shifts of the titled compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06049009
Source datasetuspto-grants-2000_04
ORD IDord-fb051fc5d06644d7a20177fb8b85879c
Source noteuspto-grants-2000_04