Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672252Generated: November 1, 2026

Hydrochloric Acid → HCID 67332127, compound

https://huagongshe.com/reaction/1672252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 45496562HCID 45496562—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67332127HCID 6733212731%

Reaction Conditions

Temperature-20 °C

Reaction Steps

2-[(Biphenyl-4-carbonyl)-amino]-pentanedioic acid 5-methyl ester (1.128 g, 3.30 mmol, 1.0 equiv.) was dissolved in THF (35 mL). The mixture was cooled to −20° C., followed by the addition of Et3N (343 mg, 3.3 mmol, 1.0 equiv.) and ethyl chloroformate (358 mg, 3.3 mmol, 1.0 equiv.). After stirring for 20 minutes, NaBH4 (375 mg, 9.9 mmol, 3 equiv.) was added and the temperature was raised to −10° C. After stirring for 5 min, MeOH (30 mL) was introduced and the mixture was further stirred for 20 min at this temperature and then at 0° C. for 20 min. 1N HCl was then added slowly to quench the reaction. Solvent was evaporated and the residue partitioned between EtOAc and H2O. The organic layer was washed with brine, dried over MgSO4, and removed solvent by rotavap. The crude mixture was then purified by column chromatography (silica gel, 3% MeOH/CH2Cl2) to afford 333 mg of 4-[(Biphenyl-4-carbonyl)-amino]-5-hydroxy-pentanoic acid methyl ester in 31% yield. MS (ESI) m/z 328.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998965B2
Source datasetuspto-grants-2011_08
ORD IDord-5294b7280fa54f158e30c2169eb1d9db
Source noteuspto-grants-2011_08