HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649349Generated: October 30, 2026
Allyl Mercaptan → HCID 20143887, compound
https://huagongshe.com/reaction/649349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Mercaptan | HCID 13367 | — |
| Reactant | Butanoic acid, 4-chloro-, methyl ester | HCID 76612 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20143887 | HCID 20143887 | — |
Reaction Steps
Into a 1 liter flask equipped with cooling bath, thermometer, reflux condenser and additional 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04739105 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-9a77734ffd654bfdaba0e8020b545b27 |
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| Source note | uspto-grants-1988_04 |
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