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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMorpholineHCID 8083—
ReactantEthyl 2-benzyl-3-chlorosulphonylpropionateHCID 21475177—
SolventDichloromethaneHCID 6344—
Productethyl (RS)-alpha-[(morpholinosulphonyl)methyl]-hydrocinnamateHCID 8675163492.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688946
Source datasetuspto-grants-1997_11
ORD IDord-6bbb31e86af74ffa9f51accdb3a983c7
Source noteuspto-grants-1997_11