HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504829Generated: October 27, 2026
Triethylamine → ethoxycarbonyl N-(tert-butoxycarbonyl)-S-methylcysteinate
https://huagongshe.com/reaction/1504829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Boc-cys(ME)-OH | HCID 7018744 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethoxycarbonyl N-(tert-butoxycarbonyl)-S-methylcysteinate | HCID 86731709 | — |
Reaction Steps
To a solution of N-(tert-butoxycarbonyl)-S-methylcysteine (23.5 g, 0.100 mol) in THF (400 mL) was added dropwise ethylchloroformate (9.6 mL, 0.10 mol) and triethylamine (10.1 g, 0.100 mol) slowly at −10° C. The reaction mixture was stirred at −10° C. for 30 minutes, and then the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to give ethoxycarbonyl N-(tert-butoxycarbonyl)-S-methylcysteinate which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216173B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-7e9000d3f83b43d3a06bff4ccc40ff3c |
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| Source note | uspto-grants-2015_12 |
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