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Sulfuryl chloride → HCID 68656860、化合物

HRID 1626980
ノート
印刷プレビュー

反応式

HRID 1626980 の反応式
[CH:1]1([CH2:4][N:5]2[C:9]3[CH:10]=[CH:11][C:12]([O:14][CH3:15])=[CH:13][C:8]=3[N:7]=[N:6]2)[CH2:3][CH2:2]1.S(Cl)([Cl:19])(=O)=O>C(O)(=O)C.C(OCC)(=O)C>[Cl:19][C:13]1[C:8]2[N:7]=[N:6][N:5]([CH2:4][CH:1]3[CH2:2][CH2:3]3)[C:9]=2[CH:10]=[CH:11][C:12]=1[O:14][CH3:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24648Sulfuryl chlorideHCID 686570341-(cyclopropylmethyl)-5-methoxy-1H-benzotriazole

生成物 1

HCID 68656860HCID 68656860、化合物

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

1-(Cyclopropylmethyl)-5-methoxy-1H-benzotriazole (10 g, 49 mmol) was dissolved in acetic acid (100 mL), cooled to 0° C. and treated with sulfuryl dichloride (4.8 mL, 59 mmol, 1.2 equiv) over three minutes. The mixture was warmed to ambient temperature over three hours and stirred for an additional 14 hours. The mixture was diluted with ethyl acetate and washed with aqueous saturated sodium bicarbonate. The organic layer was dried with magnesium sulfate, filtered and partially concentrated in vacuo to ˜30 mL, which was then treated with water. The resulting precipitate was filtered, collected and dried in vacuo, providing the titled compound.

後処理

  1. temperatureThe mixture was warmed to ambient temperature over three hours
  2. washwashed with aqueous saturated sodium bicarbonate
  3. dry with materialThe organic layer was dried with magnesium sulfate
  4. filtrationfiltered
  5. concentrationpartially concentrated in vacuo to ˜30 mL, which
  6. additionwas then treated with water
  7. filtrationThe resulting precipitate was filtered
  8. customcollected
  9. customdried in vacuo

出典と根拠

ORDレコード
ord-00bf68d0b528405b94094f00636751c0
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785482B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート