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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732443Generated: November 1, 2026

Water → 1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene

https://huagongshe.com/reaction/1732443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
ReactantBenzaldehyde, 4-(2-methylpropyl)-HCID 577537—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
Product1-Methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethyleneHCID 5456261287.2%

Reaction Steps

p-Isobutylbenzaldehyde (486 mg) and 450 mg of formaldehyde dimethyl mercaptal S-oxide were dissolved in 1 ml of t-butanol, and 2.0 ml of a 0.608 N t-butanol solution of potassium t-butoxide was added. The mixture was stirred at room temperature for 12 hours. Water (0.5 ml) and 50 ml of methylene chloride were added to the reaction mixture. The resulting mixture was dried over anhydrous sodium sulfate. The drying agent and the insoluble matter were removed by filtration, and the filtrate was concentrated under reduced pressure. The oily residue was chromatographed on a silica gel column using methylene chloride as an eluant to afford 701 mg of 1-methylsulfinyl-1-methylthio-2-(p-isobutylphenyl)ethylene in a yield of 87%. Samples for analysis were obtained by simple distillation of this product (at a bath temperature of 160° to 170° C./0.02 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237298
Source datasetuspto-grants-1980_12
ORD IDord-fd26c2ca74fd4980bdf96f8eb6b75808
Source noteuspto-grants-1980_12