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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741979Generated: October 30, 2026

Dimethyl Sulfide → HCID 53660136, compound

https://huagongshe.com/reaction/1741979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantSodium ChlorideHCID 5234—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 131718634HCID 131718634—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 53660136HCID 5366013695.3%

Reaction Conditions

Temperature-25 °C

Reaction Steps

N-chlorosuccinimide (140 mg) was suspended in 10 ml of methylene chloride, and 74 mg of dimethyl sulfide was added at 0° C. The mixture was stirred, and cooled to -25° C. A solution of 958 mg of (4-(3-tert-butyldiphenylsilyloxypropoxy)-3,5-bis-(tert -butyldiphenylsilyloxy)-2-methylenecyclohexylidene) ethanol in 2 ml of methylene chloride was added dropwise, followed by stirring at 0° C. for 2 hours. A sodium chloride aqueous solution was added to the reaction mixture, and extraction was conducted with diethyl ether. The extract was washed with a sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. There resulted 931 mg of (4-(3-tert-butyldiphenylsilyloxypropoxy)-3,5-bis-(tert-butyldiphenylsilyloxy)-2-methylenecyclohexylidene)ethyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334740
Source datasetuspto-grants-1994_08
ORD IDord-90de5341a4d6400195f23aa580ef857a
Source noteuspto-grants-1994_08