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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249337Generated: October 30, 2026

Allyl Mercaptan → HCID 20143887, compound

https://huagongshe.com/reaction/1249337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl MercaptanHCID 13367—
ReactantButanoic acid, 4-chloro-, methyl esterHCID 76612—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
ProductHCID 20143887HCID 20143887—

Reaction Steps

Into a 1 liter flask equipped with cooling bath, thermometer, reflux condenser and addition funnel as well as electric stirrer is placed 68.2 grams of methyl-4-chlorobutyrate. The methyl-4-chlorobutyrate is cooled to 20° C. The mixture of sodium methoxide and allyl mercaptan is added to the addition funnel. Over a period of 0.5 hours while maintaining the pot temperature at 20°-30° C., the mixture of allyl mercaptan and sodium methoxide is added slowly to the methyl-4-chlorobutyrate with stirring. The reaction is exothermic and requires slight cooling. At the end of the addition of the mixture of allyl mercaptan and sodium methoxide, the reaction mass is stirred for 1 hour and the temperature of the reaction mass is permitted to rise to 38° C. 500 ml water are then added to the reaction mass and the reaction mass is transferred to a separatory funnel. The reaction mass is then extracted with three 50 ml portions of methylene dichloride and dried over anhydrous sodium sulfate and filtered. The reaction mass is then distilled on a micro Vigreux column yielding the following fractions:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04631194
Source datasetuspto-grants-1986_12
ORD IDord-687bad3f8cff4a5790dc970a3e44c3a7
Source noteuspto-grants-1986_12