Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857169Generated: November 2, 2026

Water → Tert-butyl 3-(4-cyanophenoxy)-2-hydroxypropylcarbamate

https://huagongshe.com/reaction/857169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4-[(3-Amino-2-hydroxypropyl)oxy]benzonitrileHCID 16782739—
SolventTetrahydrofuranHCID 8028—
ProductDiisopropyl EtherHCID 7914—
ProductTert-butyl 3-(4-cyanophenoxy)-2-hydroxypropylcarbamateHCID 21867654148.7%

Reaction Steps

A cooled (0° C.) solution of 4-[(3-amino-2-hydroxypropyl)oxy]benzonitrile (from step (b) above; 44.6 g, 0.23 mol) in THF:H2O (1.5 L of 1:1) was treated with di-tert-butyl dicarbonate (53 g, 0.24 mol). The mixture was stirred at rt overnight, after which NaCl was added and the resulting organic layer separated. The water layer was extracted with ether and the combined organics were dried and concentrated in vacuo. The resulting oil (70 g) was filtered through a plug of silica, and then crystallised from diethyl ether:di-iso-propyl ether to yield 50 g of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144914B2
Source datasetuspto-grants-2006_12
ORD IDord-d6d3f9eb287c4f1ab2627849f7b6dcf0
Source noteuspto-grants-2006_12