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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830139Generated: October 30, 2026

Benzyl mercaptan → HCID 22054015, compound

https://huagongshe.com/reaction/1830139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
Reactant2-benzylsulfanylmethyl-N-isopropyl-succinamic acidHCID 22054079—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22054015HCID 22054015—

Reaction Steps

To a stirring mixture of itacconic anhydride (1.1209 g, 10 mmol) in 10 ml of methylene chloride at 0° C. was added drop wise isopropyl amine (0.85 ml, 10 mmol). The reaction was stirred at room temperature for 1 hour and the solvent was removed under reduced pressure to give 2-(isopropylcarbamoyl-methyl)-acrylic acid. The residue was dissolved in 10 ml of DMF, then benzyl mercaptan (1.17 g, 10.0 mmol) and DMAP (122 mg, 1 mmol) were added and the reaction was stirred at room temperature for overnight. The mixture containing 2-benzylsulfanylmethyl-N-isopropyl-succinamic acid was cooled to 0° C. and oxone® (4.9182 g, 8 mmol) in 20 ml of water was added and stirred for 2 hours at room temperature. More oxone® was added and the reaction was stirred at room temperature for 18 hours. The reaction was filtered and the white solid was washed with water, ether and dried under high vacuum to give 1.0 grams of N-isopropyl-2-benzylsulfonylmethyl-succinamic acid, which was used without further purification; LCMS retention time 2:32 minutes: MS+1 (328.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064123B1
Source datasetuspto-grants-2006_06
ORD IDord-f8e70ac6400f48d099389c7d2c043092
Source noteuspto-grants-2006_06