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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459109Generated: October 25, 2026

Acetic Acid → N-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanol

https://huagongshe.com/reaction/1459109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantN-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl esterHCID 22940772—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductN-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanolHCID 67688130—

Reaction Steps

4.15 g (11.2 mmol) of N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester is dissolved in 20 ml of tert-butyl methyl ether and mixed with 0.17 g (4.5 mmol) of sodium borohydride. At 0° C., 6 ml of methanol is added and it is stirred for three hours under argon at a temperature below 5° C. Then, 0.8 ml of acetic acid, dissolved in 3 ml of tetrahydrofuran, is added, mixed with 3 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 (eluent: ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05853699
Source datasetuspto-grants-1998_12
ORD IDord-ca274c22274d40b7a345efc0e30b3f31
Source noteuspto-grants-1998_12