HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465049Generated: October 29, 2026
Sodium Carbonate → (S)-chloromethyl 2-((tert-butoxycarbonyl)amino)propanoate
https://huagongshe.com/reaction/1465049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | Chloromethyl chlorosulfate | HCID 2733556 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-chloromethyl 2-((tert-butoxycarbonyl)amino)propanoate | HCID 11481803 | — |
Reaction Steps
To a vigorously stirred mixture of (S)-2-((tert-butoxycarbonyl)amino) propanoic acid (1 g, 5.29 mmol), tetrabutylammonium hydrogen sulfate (0.359 g, 1.057 mmol), and Na2CO3 (2.80 g, 26.4 mmol) in DCM 20 (mL) and water (20 mL), cooled in an ice/water bath, was slowly added chloromethyl chlorosulfate (1.09 mL, 10.57 mmol) over a 4 min period. After stirring in an ice/water bath for 30 min, the cold bath was removed and the reaction mixture was allowed to stir at room temperature. After stirring 16 h at room temperature the reaction mixture was diluted with water and extracted with DCM. The aqueous layer was back extracted with DCM and the combined organic layers were dried over MgSO4, filtered and concentrated. The crude material (1.64 g) was used as is without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999918B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-2731a64987724356a1d7285f23af7bcb |
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| Source note | uspto-grants-2015_04 |
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