Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661746Generated: October 29, 2026

Sodium borohydride → Tert-butyl (1-(3-ethoxy-4-methoxyphenyl)-3-hydroxybutyl)carbamate

https://huagongshe.com/reaction/1661746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl (1-(3-ethoxy-4-methoxyphenyl)-3-oxobutyl)carbamateHCID 67175760—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl (1-(3-ethoxy-4-methoxyphenyl)-3-hydroxybutyl)carbamateHCID 131724264—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A mixture of (tert-butoxy)-N-[1-(3-ethoxy-4-methoxyphenyl)-3-oxobutyl]carboxamide (2.0 g, 5.92 mmol) and sodium borohydride (0.4 g, 12.0 mmol) in methanol (40 mL) and tetrahydrofuran (10 mL) was stirred at −10 to −20° C. for 4 hours. The mixture was quenched with water (10 mL) and then concentrated in vacuo to afford an oil. The oil was dissolved in ethyl acetate and washed with water, brine, dried, and concentrated in vacuo to afford an oil. The oil was purified by chromatography (silica gel, methylene chloride:ethyl acetate 8:2) to give the two diasteromers of (tert-butoxy)-N-[1-(3-ethoxy-4-methoxyphenyl)-3-hydroxybutyl)carboxamide:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030343B2
Source datasetuspto-grants-2011_10
ORD IDord-b0447d441af740cb9b0a2b623cf9a64a
Source noteuspto-grants-2011_10