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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786435Generated: October 29, 2026

Hydrochloric Acid → HCID 58458990, compound

https://huagongshe.com/reaction/1786435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(S)-Benzyloxycarbonylamino-cyclopropyl-acetic acidHCID 67033893—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58458990HCID 5845899050%

Reaction Steps

A solution of (S)-benzyloxycarbonylamino-cyclopropyl-acetic acid (3.2 g, 12.8 mmol) in THF (20 mL) was cooled in an ice/water bath and treated with a 1 M solution of BH3 in THF (16.7 mL, 16.7 mmol). The reaction was stirred for 4 hours and then treated with 1 M HCl until the bubbling ceased. The reaction was stirred overnight and the organic solvent was removed by rotary evaporation. The residue was treated with ethyl acetate and transferred to a separatory funnel. The aqueous phase was discarded and the organics were washed twice with 1 M NaOH, dried over MgSO4 and the solvent was removed. The residue was purified on silica gel using a gradient of 0-100% ethyl acetate in hexane to afford 1.5 g (50% yield) of (S)-(1-Cyclopropyl-2-hydroxy-ethyl)-carbamic acid benzyl ester as a white solid; 1H NMR (CDCl3, 400 MHz) δ 0.26-0.37 (m, 1H), 0.34-0.44 (m, 1H), 0.47-0.61 (m, 2H), 0.83-0.94 (m, 1H), 2.95-3.04 (m, 1H), 3.70 (dd, 1H, J1=5.8, J2=11.1), 3.79-3.88 (m, 1H), 5.00-5.12 (m, 1H), 5.10 (s, 2H), 7.29-7.31 (m, 5H); HPLC-MS calcd. for C13H17NO3 (M+H+) 236.1, found 236.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507755B2
Source datasetuspto-grants-2009_03
ORD IDord-f24672f96fd449ec889e1ebcdbfb4b43
Source noteuspto-grants-2009_03