Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915103Generated: November 2, 2026

Methyl chloroformate → 4-(tert-Butyl)-2-(2-cyanopropan-2-yl)phenyl methyl carbonate

https://huagongshe.com/reaction/1915103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(5-(tert-Butyl)-2-hydroxyphenyl)-2-methylpropanenitrileHCID 59544165—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-(tert-Butyl)-2-(2-cyanopropan-2-yl)phenyl methyl carbonateHCID 59544146—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of compound 15 (126.6 g, 0.564 mol), DMAP (6.0 g) and DIEA (188 g, 1.46 mol) in anhydrous DCM (1500 mL) was added dropwise methyl chloroformate (110 g, 1.17 mol) in anhydrous DCM (300 mL) at 0° C. within 2 hours. After stirring for 12 hours at 0° C., ice-water (1.5 L) was added and the mixture was stirred at 0° C. for 30 minutes. The organic layer was separated and washed with 1 N HCl, water, and brine. The DCM solution was dried over MgSO4 and concentrated in vacuo to give compound 16 as a yellow solid. 1H NMR (DMSO-d6; 400 MHz) δ 7.47 (m), δ 7.39 (d), δ 7.24 (d), δ 3.84 (s), δ 1.71 (s), δ 1.30 (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614325B2
Source datasetuspto-grants-2013_12
ORD IDord-2c60be44ecb54691848f8329e18f3d5d
Source noteuspto-grants-2013_12