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HRID 34526作成日:2026年10月25日

Iodine → Dimethyl-4-tert-butylbenzylchloromethylsilane

https://huagongshe.com/reaction/34526

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Ammonium ChlorideHCID 25517—
反応物Silane, chloro(chloromethyl)dimethyl-HCID 74393—
反応物Benzene, 1-(chloromethyl)-4-(1,1-dimethylethyl)-HCID 88198—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物Dimethyl-4-tert-butylbenzylchloromethylsilaneHCID 70420968—

反応手順

1.2 g (0.05M) of magnesium shavings are charged into 20 ml of diethyl ether. After the addition of about 1 ml of 4-tert-butylbenzyl chloride, the batch is heated to boiling point and a number of iodine crsytals are added. After the onset of the reaction, the rest of the 4-tert-butylbenzyl chloride (a total of 10 g [0.055M] in 80 ml of diethyl ether) is added dropwise such that the temperature is kept at 25°-30° C. The reaction mixture is stirred further for 2 hours at room temperature. 7.2 g (0.05M) of chloromethyldimethylchlorosilane in 20 ml of diethyl ether are then added dropwise at room temperature, and the mixture is stirred further overnight at room temperature. With ice cooling, 100 ml of a saturated solution of ammonium chloride are added to the reaction mixture, and the organic phase is separated, diluted with ethyl acetoacetate and washed three times with water. The batch is dried over sodium sulfate and filtered, and the filtrate is concentrated under a water jet vacuum. The crude intermediate so obtained is cooled to 0° C. and filtered, affording 11.2 g (88% of theory) of the desired intermediate as filtrate. For further purification, the product can be distilled under a water jet vacuum (boiling point: 149°-150° C./2000 Pa).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04762826
出典データセットuspto-grants-1988_08
ORD IDord-f442658e4b114f5dacca10509b95b8b9
出典メモuspto-grants-1988_08