Thiophosgene → 2-Chloro-6-fluorophenylisothiocyanate
반응식
[Cl:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([F:9])[C:3]=1[NH2:4].[C:10](Cl)(Cl)=[S:11].C(N(C(C)C)C(C)C)C>>[Cl:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([F:9])[C:3]=1[N:4]=[C:10]=[S:11]참가 물질
4
실험 절차
The title compound was prepared following the procedure described for intermediate-2 using 2-chloro-6-fluoro aniline (3.0 g, 19.35 mmol), thiophosgene (5.01 g, 43.47 mmol) and N-ethyl di-isopropyl amine (8.0 g, 64.00 mmol) to afford 1.0 g of the desired product. 1HNMR (DMSO-d6): δ 7.26 (m, 2H), 7.06 (t, J=9.6 Hz, 1H).
후처리
- customThe title compound was prepared
출처 및 근거
- ORD 기록
- ord-11a536e4c23740aba11eac6e8170db41
- 출처 데이터셋
- uspto-grants-2013_08
- 특허 번호
- US08519149B2
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