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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732442Generated: November 3, 2026

Benzaldehyde → HCID 53914774, compound

https://huagongshe.com/reaction/1732442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethanolHCID 887—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53914774HCID 5391477491%

Reaction Steps

FAMSO (2.572 g), 3 ml of a 40% methanol solution of trimethylbenzylammonium hydroxide, and 3 ml of benzaldehyde were added to 5 ml of tetrahydrofuran, and the mixture was refluxed for 4 hours. After adding 100 ml of methylene chloride, the reaction mixture was washed with dilute sulfuric acid. The product was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was chromatographed on a silica gel using methylene chloride as an eluant to afford 3.994 g of 1-methylsulfinyl-1-methylthio-2-phenylethylene as a colorless liquid having a boiling point of 149° to 150° C./0.08 mmHg in a yield of 91.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237298
Source datasetuspto-grants-1980_12
ORD IDord-e3248e17148e463584011251e5c10cf0
Source noteuspto-grants-1980_12