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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265702Generated: October 26, 2026

Ammonia → 1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine

https://huagongshe.com/reaction/265702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium CarbonateHCID 10340—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1H-Pyrrole, 1-benzoyl-2,5-dihydro-HCID 11252283—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidineHCID 70282017—

Reaction Steps

41.5 g (0.24 mol) of 1-benzoyl-2,5-dihydropyrrole are initially introduced into 240 ml of methylene chloride, and 24.8 g (0.3 mol) of methanesulphonyl chloride are added dropwise at 0° C. The mixture is subsequently stirred at room temperature for 16 hours, the solvent is then stripped off under 8 mbar and the residue is taken up in 240 ml of tetrahydrofuran. After addition of 65 g of 25% strength ammonia solution, the mixture is heated at 80° C. in an autoclave for 10 hours. It is then poured into 5 times the amount of water, the pH is brought to 10-11 with sodium carbonate, the mixture is extracted with methylene chloride and the extract is dried over sodium sulphate and concentrated. The crude product (50 g) is chromatographed on silica gel (mobile phase initially ethanol:ethyl acetate 1:3, then ethanol; Rf value: 0.34 ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648493
Source datasetuspto-grants-1997_07
ORD IDord-3cd7799624fd4c2fb0848aab196067d2
Source noteuspto-grants-1997_07