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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-N-Boc-aminopropionic acidHCID 268471—
ReactantSodium BicarbonateHCID 516892—
ReactantChloromethyl chlorosulfateHCID 2733556—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 72978647HCID 7297864797%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354421B2
Source datasetuspto-grants-2013_01
ORD IDord-453dc1d33c844905bb52bc3783411f8a
Source noteuspto-grants-2013_01