참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Disulfide | HCID 12232 | — |
| 반응물 | 1-Chloro-3-fluorobenzene | HCID 223087 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | (2-Chloro-6-fluorophenyl)(methyl)sulfane | HCID 53633719 | 126.7% |
반응 단계
n-Butylithium (2.5M in hexane, 129 ml) was added to a solution of 3-fluorochlorobenzene (35 g) in dry tetrahydrofuran while maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 3 hours and dimethyl disulphide (60.65 g) was added. The mixture was allowed to warm to room temperature and stirred overnight. The mixture was evaporated to dryness and the residue was suspended in ether and washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 2-chloro-6-fluorothioanisole (60 g) as a crude yellow oil containing some dimethyl disulphide, NMR (CDCl3) 2.45(s,3H), 6.95(t,1H), 7.1-7.3(m,2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05856274 |
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| 출처 데이터셋 | uspto-grants-1999_01 |
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| ORD ID | ord-74d29cbdb4b64b6a9fac27f6d8a4488d |
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| 출처 메모 | uspto-grants-1999_01 |
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