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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409871Generated: October 29, 2026

Triethylamine → HCID 57947489, compound

https://huagongshe.com/reaction/409871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 141232704HCID 141232704—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57947489HCID 5794748980.1%

Reaction Steps

To a mixture of (S)-2-((benzyloxycarbonyl)(methyl)amino)-4-tert-butoxy-4-oxobutanoic acid dicyclohexylammonium salt (20 g, 0.0386 mol) and Et3N (7.90 mL, 0.0579 mol) in THF (500 mL) was added isobutyl chloroformate (6.05 mL, 0.0463 mol) at 0° C. The reaction mixture was stirred for 1 h, and filtered to remove TEA salt. To the filtrate was added a solution of NaBH4 (2.19 g, 0.0579 mol) in THF (50 mL) and water (100 mL) at 0-5° C. The reaction mixture was stirred at RT for 1 h and quenched with saturated NH4Cl solution. The reaction mixture was concentrated to remove most of THF and extracted with EtOAc (700 mL×3). The organic layers were washed with water, NaHCO3 and brine, dried over Na2SO4, and concentrated to give (S)-tert-butyl 3-((benzyloxycarbonyl)(methyl)amino)-4-hydroxybutanoate (10 g), which was used without further purification. LRMS (M+Na+) m/z 346.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759374B2
Source datasetuspto-grants-2014_06
ORD IDord-512767a163384b43852bce9eb1916e98
Source noteuspto-grants-2014_06