HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446138Generated: October 29, 2026
Methyl chloroformate → 4-(tert-Butyl)-2-(2-cyanopropan-2-yl)phenyl methyl carbonate
https://huagongshe.com/reaction/446138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(5-(tert-Butyl)-2-hydroxyphenyl)-2-methylpropanenitrile | HCID 59544165 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(tert-Butyl)-2-(2-cyanopropan-2-yl)phenyl methyl carbonate | HCID 59544146 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476442B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ab4845de239043d0897673056ad46a9d |
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| Source note | uspto-grants-2013_07 |
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