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Sulfuryl chloride → HCID 68656860, 화합물

HRID 872285
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HRID 872285 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

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

생성물 1

HCID 68656860HCID 68656860, 화합물

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

1-(Cyclopropylmethyl)-5-methoxy-1H-benzotriazole (8-3, 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 8-4.

후처리

  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

출처 및 근거

ORD 기록
ord-71682321c92e4af6bbf37a67c4798946
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08975286B2

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