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Thiophosgene → 2,6-Dichloro-3-methoxyphenylisothiocyanate

HRID 1902867
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HRID 1902867 반응식
[Cl:1][C:2]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[C:5]([Cl:11])[C:3]=1[NH2:4].[C:12](Cl)(Cl)=[S:13]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[C:5]([Cl:11])[C:3]=1[N:4]=[C:12]=[S:13]
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참가 물질

4

반응물 2

HCID 10040ThiophosgeneHCID 205138882,6-Dichloro-3-methoxyaniline

생성물 1

HCID 205138492,6-Dichloro-3-methoxyphenylisothiocyanate

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

60.7 g of 2,6-dichloro-3-methoxy-aniline are dissolved in 65 ml of toluene and treated with 25 ml of thiophosgene in 50 ml of toluene. The solution obtained is heated to boiling under reflux overnight and subsequently evaporated in vacuo. There is obtained 2,6-dichloro-3-methoxyphenylisothiocyanate of boiling point 99° (0.13 Torr).

후처리

  1. customThe solution obtained
  2. temperatureis heated
  3. temperatureunder reflux overnight
  4. customsubsequently evaporated in vacuo

출처 및 근거

ORD 기록
ord-3a1c97d5615a48b19d26889ac3cf7360
출처 데이터셋
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04366160

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