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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459119Generated: November 2, 2026

Acetic Acid → HCID 67656892, compound

https://huagongshe.com/reaction/1459119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22940768HCID 22940768—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 67656892HCID 67656892—

Reaction Steps

7.9 g (22 mmol) of N-benzyloxycarbonyl-3-[2-ethoxyphenyl]-alanine-methyl ester (Example b) is dissolved in 63 ml of tert-butyl methyl ether and mixed with 1.1 g (30.1 mmol) of sodium borohydride. At 5° C., 15 ml of methanol is added, and it is stirred for five hours at constant temperature. Then, 1.5 ml of acetic acid, dissolved in 5 ml of tetrahydrofuran, is added, mixed with 9 ml of water and stirred for ten minutes at room temperature. The organic phase is separated, washed with water and dried on sodium sulfate. The drying agent is suctioned off, the filtrate is concentrated by evaporation and the residue is chromatographed for purification on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05853699
Source datasetuspto-grants-1998_12
ORD IDord-530da1809e00454599f137d613615939
Source noteuspto-grants-1998_12