HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294689Generated: November 1, 2026
Hydrochloric Acid → ethyl (RS)-alpha-[(morpholinosulphonyl)methyl]-hydrocinnamate
https://huagongshe.com/reaction/2294689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Ethyl 2-benzyl-3-chlorosulphonylpropionate | HCID 21475177 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl (RS)-alpha-[(morpholinosulphonyl)methyl]-hydrocinnamate | HCID 86751634 | 92.8% |
Reaction Steps
6.6 g (75.8 mmol) of morpholine are added dropwise at -10° to a solution of 6.23 g (21.4 mmol) of ethyl 2-benzyl-3-chlorosulphonyl-propionate (EPA 0236734) in 150 ml of methylene chloride. The solution is stirred at -10° for 1 hour and at 0° for 1 hour and subsequently acidified with 1N hydrochloric acid. The organic phase is then extracted with 50 ml of water, dried over sodium sulphate and evaporated. For purification, the residue (7.64 g) is chromatographed on 300 g of silica gel using methylene chloride as the eluent. There are obtained 6.78 g of ethyl (RS)-α-[(morpholinosulphonyl)methyl]-hydrocinnamate as a colourless oil; MS: 341 (M)+. This is converted into (S)-α-[(morpholinosulphonyl)methyl]hydrocinnamic acid by enzymatic hydrolysis using α-chymotrypsin in an analogous manner to that described in Example 1(d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688946 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-6bbb31e86af74ffa9f51accdb3a983c7 |
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| Source note | uspto-grants-1997_11 |
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