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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275861Generated: November 1, 2026

Acetic Acid → HCID 86757828, compound

https://huagongshe.com/reaction/275861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54566062HCID 54566062—
SolventMethanolHCID 887—
ProductHCID 86757828HCID 86757828—

Reaction Conditions

Temperature60 °C

Reaction Steps

In methanol (6 ml) were dissolved 2-amino-α-(3-tert-butoxycarbonylaminomethylphenyl)-5-methyloxybenzyl alcohol (0.18 g), 4-benzyloxy-benzaldehyde (0.12 g) and acetic acid (0.02 g). To the solution was added sodium cyano borohydride (0.02 mg). The mixture was stirred for 30 minutes at 60° C. The reaction mixture was concentrated, to which were added ethyl acetate (30 ml) and water (50 ml). The mixture was shaken. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by means of a silica gel column chromatography to give 2-(4-benzyloxybenzyl)-α-(3-tert-butoxycarbonylaminomethylphenyl-5-methyloxybenzyl alcohol as a colorless crystalline product (0.17 g). m.p.:86-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352982B1
Source datasetuspto-grants-2002_03
ORD IDord-6ce62d59793548aa9159795263862f1d
Source noteuspto-grants-2002_03