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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180444Generated: October 26, 2026

Trichloroacetonitrile → (4-Bromophenyl)(phenyl)methyl 2,2,2 trichloroethanimidoate

https://huagongshe.com/reaction/1180444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetonitrileHCID 11011—
ReactantSodium hydrideHCID 24758—
Reactantp-Bromobenzhydryl alcoholHCID 98221—
SolventDiethyl EtherHCID 3283—
Product(4-Bromophenyl)(phenyl)methyl 2,2,2 trichloroethanimidoateHCID 69473260—

Reaction Conditions

Temperature0 °C

Reaction Steps

(4-bromophenyl)(phenyl)methanol from example 67 step 2 (175 g, 0.665 mol) was dissolved in Et2O (700 mL) and sodium hydride (2.66 g of 60% dispension in oil, 0.067 mol, 0.1 eg) was added. Reaction mixture was cooled to 0° C. and trichloroacetonitrile (96 g, 0.665 mol, 1 eg) was added dropwise over 15 min. Reaction mixture was allowed to warm to room temperature and stirred for 1.5 hours. Mixture was evaporated to dryness and solid was stirred in hexane for 18 hours. The solid was filtered to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279478B2
Source datasetuspto-grants-2007_10
ORD IDord-d6773aef15e24433a995ccf9c597147b
Source noteuspto-grants-2007_10