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HRID 128511作成日:2026年10月27日

Oxalyl chloride → Benzeneacetyl chloride, 4-bromo-

https://huagongshe.com/reaction/128511

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物Benzeneacetic acid, 4-bromo-HCID 74654—
反応物6-Bromo-2-tetraloneHCID 2733553—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Benzeneacetyl chloride, 4-bromo-HCID 181552—

反応手順

The synthesis of 6-bromo-2-tetralone is accomplished by dissolving 4-bromophenylacetic acid in methylene chloride and dimethyl formamide, under nitrogen. Oxalyl chloride is added and the mixture is stirred under a positive nitrogen atmosphere to produce the 4-bromo-phenylacetyl chloride, at a yield which typically is better than 99%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464762
出典データセットuspto-grants-1995_11
ORD IDord-76ffd24e304642158af2cc014d8e9207
出典メモuspto-grants-1995_11