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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70943Generated: October 24, 2026

4-Phenoxybenzoyl chloride → N-[2-(4-Chloro-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamide

https://huagongshe.com/en/reaction/70943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxybenzoyl chlorideHCID 74193—
Reactant2-amino-3-(4-chloro-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66620057—
ProductN-[2-(4-Chloro-2H-benzotriazol-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamideHCID 66620748—

Reaction Steps

Using a procedure similar to that described in Example 1, except using 2-amino-3-(4-chloro-2H-benzotriazol-2-yl)-2-methylpropionitrile (100 mg, described in Example 35) and 4-phenoxybenzoyl chloride (0.10 mL), the title compound was isolated as a white solid (70 mg, 38%). Rf=0.7 (1:1 EA/heptane). MS (ES): M/Z [M+H]=432. NMR: (400 MHz, DMSO-d6): 1.75 (s, 3H), 5.43 (d, J=13.3 Hz, 1H), 5.50 (d, J=13.3 Hz, 1H), 7.04-7.10 (m, 4H), 7.22 (t, J=7.4 Hz, 1H), 7.43-7.48 (m, 3H), 7.59 (d, J=6.6 Hz, 1H), 7.84 (d, J=8.9 Hz, 2H), 7.94 (d, J=8.0 Hz, 1H) and 8.73 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822689B2
Source datasetuspto-grants-2014_09
ORD IDord-2acb7fc34287407db16f9a9da77ddd4e
Source noteuspto-grants-2014_09