HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326753Generated: October 26, 2026
Triethylamine → 4-(t-Butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine
https://huagongshe.com/reaction/326753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-(tert-Butoxycarbonyl)thiomorpholine-3-carboxylic acid | HCID 2756831 | — |
| Reactant | Ethyl cyanophosphate | HCID 86180093 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(t-Butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine | HCID 15730145 | 74% |
Reaction Steps
Triethylamine (3.1 ml), 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)thiomorpholine3-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270327 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-bf509a1480514a31bae5d06696ba1bd3 |
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| Source note | uspto-grants-1993_12 |
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