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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271007Generated: October 28, 2026

Acetic Acid → HCID 69972127, compound

https://huagongshe.com/reaction/2271007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolamineHCID 700—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 56982192HCID 56982192—
SolventMethanolHCID 887—
ProductHCID 69972127HCID 6997212782.6%

Reaction Steps

A solution of (3S)-4-benzyloxy-3-tert-butoxycarbonylamino-2-butanone (4.3 g) in dry MeOH (20 ml) was added to a solution of 2-aminoethanol (2.0 g) and AcOH (1.8 g) in dry MeOH (20 ml). NaBH3CN (1.4 g) was added and the mixture was stirred at ambient temperature overnight. The mixture was concentrated in vacuo and the residue was partitioned between AcOEt and aqueous NaHCO3 solution. The organic layer was washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution. The organic layer was mixed with 1N HCl (50 ml) and the mixture was stirred vigorously for 1 hour. The organic layer was separated, washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution, dried over MgSO4 and concentrated in vacuo to give 4.1 g of (2R, 3RS)-O-benzyl-2-tert-butoxycarbonylamino-3-(2-hydroxyethylamino)butanol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333324B1
Source datasetuspto-grants-2001_12
ORD IDord-3a6f09165131441f9627d230631cb5da
Source noteuspto-grants-2001_12