HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609436Generated: October 31, 2026
Sulfate Ion → Methyl 3-isothiocyanatopropionate
https://huagongshe.com/reaction/1609436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfate Ion | HCID 1117 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-isothiocyanatopropionate | HCID 140454 | 89.3% |
Reaction Steps
1,256 ml of triethylamine was added to a solution of 603.6 g of β-alaninemethylester sulfate in 1.5 liter of methyl alcohol under cooling with ice. 235 ml of carbon disulfide was added dropwise to the system at a temperature of 10° C. or lower. After the dropwise addition, the system was then stirred at a temperature of 10° C. or lower for 1 hour. 288 ml of ethyl chloroformate was added dropwise to the system at a temperature of 5° C. or lower. The system was then stirred for 2 hours. After the reaction, the reaction solution was then subjected to separation with ethyl acetate and water. The ethyl acetate phase thus extracted was dried with magnesium sulfate, and then filtered off. Ethyl acetate was then distilled off from the system under reduced pressure to obtain 389.1 g (yield: 89.3%) of the desired substance in the form of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401621 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-8184e52749dd485e9dda4aab9b31e888 |
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| Source note | uspto-grants-1995_03 |
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