HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862016Generated: October 28, 2026
Ethanesulfonyl chloride → N-(Ethylsulfonyl)-D-phenylalanine
https://huagongshe.com/reaction/1862016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | D-Phenylalanine | HCID 71567 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Product | N-(Ethylsulfonyl)-D-phenylalanine | HCID 15385776 | 79% |
Reaction Steps
To a stirring suspension of D-phenylalanine (50 g, 300 mmol) in THE (400 mL) was added N,O-bis(trimethylsilyl) acetamide (92 g, 450 mmol). After stirring for 12 h, the solution was cooled to −78° C. and N,N-diisopropylethylamine (58 mL, 330 mmol) was added. To this solution was slowly added ethanesulfonyl chloride (31 mL, 330 mmol) and the cold bath was removed. After stirring for 20 h, the solvents were removed in vacuo and the residue was partitioned between saturated aqueous NaHCO3 and ethyl acetate. The aqueous phase was washed with diethyl ether, acidified with solid citric acid and extracted twice with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried with MgSO4, filtered and concentrated in vacuo to give 61 g (79%) of a thick colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06534650B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-4ed824a11c2241b98475261a810371f9 |
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| Source note | uspto-grants-2003_03 |
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