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Hydrochloric Acid → Benzene, 2-(chloromethyl)-1,4-dimethyl-

HRID 1183839
ノート
印刷プレビュー

反応式

HRID 1183839 の反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:8])=[CH:6][CH:7]=1.F[B-](F)(F)F.[CH2:14]([N+]1C=CN(C)C=1)C.[ClH:22]>O>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[CH2:14][Cl:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric Acid2 回HCID 7809P-XyleneHCID 178462726HCID 178462726、化合物

生成物 1

HCID 69987Benzene, 2-(chloromethyl)-1,4-dimethyl-収率 1,844.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

53 g p-xylene, 4.9 g 1-ethyl-3-methylimidazolium tetrafluoroborate and 1.6 g concentrated hydrochloric acid whose concentration is 36% are added into a 500 ml four-neck flask and the temperature is raised to 80˜85° C. after well stirring. And the reaction solution is kept warm tor 0.5 h after the gas of hydrochloride is inflated, and then cooled to the room temperature, standing for layering. The upper layer is organic layer while the lower layer is water layer. The water layer is dehydrated trader vacuum and the gained ionic liquid can be recycled and reused. The organic layer is transferred into a 500 ml four-neck flask and is rectified under vacuum. Alter desolventizing. 70.6 g 2,5-dimethylbenzyl chloride is finally provided (91.3%) yield).

後処理

  1. temperaturethe temperature is raised to 80˜85° C.
  2. customThe organic layer is transferred into a 500 ml four-neck flask

出典と根拠

ORDレコード
ord-68e7232ee4694f098a20b597cc0db497
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08664424B2

反応ノート

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