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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401659Generated: November 2, 2026

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

https://huagongshe.com/reaction/2401659

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 numberUS08796308B2
Source datasetuspto-grants-2014_08
ORD IDord-a0922da1d2a34c3099b2ae04520ba8ea
Source noteuspto-grants-2014_08