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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847556Generated: October 30, 2026

Sodium borohydride → tert-Butyl (3-hydroxypropyl)methylcarbamate

https://huagongshe.com/reaction/847556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10703983HCID 10703983—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Producttert-Butyl (3-hydroxypropyl)methylcarbamateHCID 1037524172.8%

Reaction Steps

To a solution of N-t-butoxycarbonyl-N-methyl-β-alanine methyl ester (3.911 g) in methanol (20 ml) and water (20 ml) was added sodium borohydride (6.81 g) portionwise at 4° C. and the mixture was stirred at room temperature for 3 hours. The solution was concentrated in vacuo, and the residue was portioned between ethyl acetate (100 ml) and 0.5 N hydrochloric acid (100 ml). The separated organic layer was washed with 0.5 N hydrochloric acid (100 ml), water (100 ml), aqueous sodium bicarbonate (100 ml), water (100 ml) and brine (100 ml) successively, and dried over magnesium sulfate. Evaporation of the solvent gave 3-(N-t-butoxycarbonyl-N-methylamino)propanol (2.48 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05142048
Source datasetuspto-grants-1992_08
ORD IDord-ce57437c610e4935b82da086e1ba0c9d
Source noteuspto-grants-1992_08