HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804686Generated: October 30, 2026
2-N-Boc-aminopropionic acid → HCID 72978647, compound
https://huagongshe.com/reaction/1804686
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-N-Boc-aminopropionic acid | HCID 268471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Chloromethyl chlorosulfate | HCID 2733556 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 72978647 | HCID 72978647 | 97% |
Reaction Steps
To a solution of 2-tert-butoxycarbonylamino-propionic acid (0.507 g, 2.68 mol), sodium bicarbonate (1.13 g, 13.4 mmol) and tetrabutylammonium hydrogen sulfate (0.090 g, 0.268 mmol) in H2O (21 mL) at 0° C. was added dichloromethane (12 mL) and the mixture was stirred vigorously. Chloromethyl chlorosulfate (0.326 mL, 3.22 mmol) in dichloromethane (7 mL) was added and the mixture was warmed to rt overnight. The reaction mixture was diluted with ethyl acetate, washed with brine, dried (MgSO4) and concentrated. The resulting oil was purified by flash column chromatography (silica gel, 0 to 30% ethyl acetate/hexane) to give a colorless oil (4) (0.6207 g, 97%). 1H NMR (300 MHz, CDCl3): 5.75 (d, J=5.4 Hz, 1H), 5.57 (d, J=5.4 Hz, 1H), 5.04 (br s, 1H), 4.28 (m, 1H), 1.37 (s, 9H), 1.32 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354421B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-453dc1d33c844905bb52bc3783411f8a |
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| Source note | uspto-grants-2013_01 |
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