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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723359Generated: November 1, 2026

Acetyl chloride → HCID 4155152, compound

https://huagongshe.com/reaction/1723359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant4'-Bromo-[1,1'-biphenyl]-4-amineHCID 279574—
SolventPyridineHCID 1049—
ProductHCID 4155152HCID 415515291.2%

Reaction Steps

[I] A solution prepared by dissolving 0.75 g of 4-amino-4'-bromobiphenyl in 10 ml of pyridine, was cooled with ice, and 1.0 g of acetyl chloride was dropwise added thereto. The mixture was stirred over a period of 30 minutes. After the completion of the reaction, the reaction solution was extracted with ethyl acetate and water. The organic layer was washed with dilute hydrochloric acid and further with a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 0.8 g of N-(4'-bromo-4-biphenylyl)acetamide as colorless crystals. [II] A solution prepared by dissolving 0.80 g of N-(4'-bromo-4-biphenylyl)acetamide obtained in step [I] in 10 ml of dimethylformamide, was dropwise added at a temperature of from 15° to 20° C. to 10 ml of a dimethylsulfoxide solution in which 0.17 g of sodium hydride (60% nujol mixture) was suspended. After the dropwise addition, the mixture was stirred at room temperature for 30 minutes, and then 0.78 g of methyl iodide was dropwise added thereto at a temperature of from 15° to 20° C. Then, the mixture was stirred for 3 hours at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861799
Source datasetuspto-grants-1989_08
ORD IDord-ac25cd8d7f064c6bbfd2c1a8a6f3744d
Source noteuspto-grants-1989_08