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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493163Generated: November 3, 2026

Water → 4-(t-Butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine

https://huagongshe.com/reaction/1493163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyrrolidineHCID 31268—
Reactant4-(tert-Butoxycarbonyl)thiomorpholine-3-carboxylic acidHCID 2756831—
ReactantEthyl cyanophosphateHCID 86180093—
SolventTetrahydrofuranHCID 8028—
Product4-(t-Butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholineHCID 1573014574%

Reaction Steps

followed by a solution of pyrrolidine (2.0 ml) in 10 ml of tetrahydrofuran, was added at 0° C. under a stream of nitrogen to a solution of 5.0 g of 4-(t-butoxycarbonyl)thiomorpholine-3-carboxylic acid in 100 ml of tetrahydrofuran. After the mixture had been stirred for I hour, a solution of 3.6 g of ethyl cyanophosphate in 10 ml of tetrahydrofuran was added to the mixture and the mixture was stirred for 5 hours. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to yield 461 g (74%) of 4-(t-butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021413
Source datasetuspto-grants-1991_06
ORD IDord-4748b780180c4bc8a2715b38a211a181
Source noteuspto-grants-1991_06