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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275851Generated: November 2, 2026

Methanol → 5-Chloro-alpha-(4-tert-butoxycarbonylaminomethylphenyl)-2-neopentylaminobenzyl alcohol

https://huagongshe.com/reaction/275851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPivalaldehydeHCID 12417—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-Amino-5-chloro-alpha-(4-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54502133—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-alpha-(4-tert-butoxycarbonylaminomethylphenyl)-2-neopentylaminobenzyl alcoholHCID 54328070100%

Reaction Steps

To a methanol (8 ml) solution of 2-amino-5-chloro-α-(4-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.83 g) were added trimethyl acetaldehyde (220 mg) and acetic acid (170 mg). The mixture was stirred for 10 minutes at room temperature, to which was added sodium cyano borohydride (160 mg). The mixture was stirred overnight at room temperature, to which was added acetic acid ethyl ester (100 ml). The mixture was washed with water and dried over anhydrous Na2SO4. The solvent was then distilled off, and the residue was purified by means of a silica gel column chromatography to give the object 5-chloro-α-(4-tert-butoxycarbonylaminomethylphenyl)-2-neopentylaminobenzyl alcohol (0.99 g) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352982B1
Source datasetuspto-grants-2002_03
ORD IDord-2efdd3ed1c3c4a8c9ffa11aebead2ebf
Source noteuspto-grants-2002_03