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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721646Generated: November 1, 2026

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

https://huagongshe.com/reaction/1721646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyrrolidineHCID 31268—
Reactant4-(tert-Butoxycarbonyl)thiomorpholine-3-carboxylic acidHCID 2756831—
ReactantEthyl cyanophosphateHCID 86180093—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(t-Butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholineHCID 1573014574%

Reaction Steps

Triethylamine (3.1 mi), 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 1 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 4.61 g (74%) of 4-(t-butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512567
Source datasetuspto-grants-1996_04
ORD IDord-5c1a827e68284e988859e979609c40df
Source noteuspto-grants-1996_04