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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483804Generated: November 1, 2026

Triethylamine → methyl N-t-butoxycarbonyl-S-[(3,4-methylenedioxy)phenyl]cysteinate

https://huagongshe.com/reaction/483804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,4-(Methylenedioxy)thiophenolHCID 2759847—
ReactantBoc-Ser(Tos)-OMeHCID 7009424—
SolventChloroformHCID 6212—
Productmethyl N-t-butoxycarbonyl-S-[(3,4-methylenedioxy)phenyl]cysteinateHCID 1865269766%

Reaction Steps

After 27.7 g of (3,4-methylenedioxy)thiophenol and 74 g of methyl N-(t-butoxycarbonyl)-O-tosyl-L-serinate were dissolved in 200 ml of chloroform, 20 g of triethylamine were added at room temperature, followed by stirring overnight. The reaction mixture was washed with water and then extracted with ethyl acetate. The extract so obtained was dried over anhydrous magnesium sulfate. After the solvent was distilled off, 49 g of crude oil were obtained. The crude oil was recrystallized from an ethyl acetatehexane system, whereby 42 g of methyl N-t-butoxycarbonyl-S-[(3,4-methylenedioxy)phenyl]cysteinate were obtained (yield: 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05227398
Source datasetuspto-grants-1993_07
ORD IDord-b7ea69842239425ca8143b0c5d4aa26f
Source noteuspto-grants-1993_07