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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009963Generated: October 30, 2026

Hydrochloric Acid → HCID 57699991, compound

https://huagongshe.com/reaction/1009963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57699891HCID 57699891—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57699991HCID 5769999178%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Ethyl chloroformate (2.45 ml, 25.6 mmol) was added at −20° C. to a stirred solution of (S)-2-tert-Butoxycarbonylamino-pentanedioic acid 1-cyclopentyl ester (6.73 g, 21.4 mmol) and N-methyl morpholine (3.05 ml, 27.8 mmol) in THF (50 ml). The reaction mixture became very thick with precipitation of a white solid. The reaction was therefore diluted further with THF (100 ml) to aid mixing and left stirring at −20° C. for 2 hours. The precipitated mass was filtered off and the filtrate was added over a period of 20 minutes to a solution of sodium borohydride (2.43 g, 64.1 mmol) in THF (20 ml) and water (5 ml) at 0° C. The reaction mixture was allowed to stir to room temperature and left for 4 hours for complete reaction. The mixture was acidified to pH 5 with 1M HCl and the THF removed under reduced pressure. The aqueous solution was extracted with EtOAc (3×100 ml) and dried over magnesium sulphate. The product was purified by column chromatography (DCM-5% MeOH/DCM) and isolated as a clear oil (5.0 g, 78%). 1H NMR (300 MHz, CDCl3), δ: 5.20 (2H, m), 4.25 (1H, m), 3.65 (2H, m), 2.00-1.57 (12H, bm), 1.47 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973181B2
Source datasetuspto-grants-2011_07
ORD IDord-5aba255585774890b79376f363c55880
Source noteuspto-grants-2011_07