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Butanethiol → HCID 90414055, 화합물

HRID 1746041
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HRID 1746041 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[OH:9].C(=O)([O-])[O-].[K+].[K+].Br[C:17]([F:23])([F:22])[C:18]([F:21])([F:20])[Br:19].C(S)CCC.[OH-].[Na+]>CN(C)C=O>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[O:9][C:17]([F:23])([F:22])[C:18]([Br:19])([F:21])[F:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 8012ButanethiolHCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 313011,2-Dibromo-1,1,2,2-tetrafluoroethaneHCID 27792842-BROMO-6-FLUOROPHENOL

생성물 1

HCID 90414055HCID 90414055, 화합물수율 76.5%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

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온도
50 °C

실험 절차

2-Bromo-6-fluorophenol (10.2 g, 53 mmol), potassium carbonate (7.3 g, 53 mmol), 1,2-dibromo-tetrafluoroethane (21 g, 80 mmol) and 1-butanethiol (1.1 g, 12 mmol) were combined in dry N,N-dimethylformamide (75 mL) and heated to 50° C. in a stirred pressure reactor. After cooling, the contents were mixed with 1.0 M sodium hydroxide (NaOH; 100 mL) and extracted three times with diethyl ether (80 mL portions). The combined extracts were washed with water (15 mL), 2.0 M NaOH (45 mL), dried (Na2SO4) and concentrated by rotary evaporation. The material was purified by silica gel chromatography eluting with hexane to afford the title compound as a clear liquid (15 g, 76%): 1H NMR (400 MHz, CDCl3) δ 7.48-7.39 (m, 1H), 7.22-7.14 (m, 2H); EIMS m/z 368.

후처리

  1. temperatureAfter cooling
  2. extractionextracted three times with diethyl ether (80 mL portions)
  3. washThe combined extracts were washed with water (15 mL), 2.0 M NaOH (45 mL)
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated by rotary evaporation
  6. customThe material was purified by silica gel chromatography
  7. washeluting with hexane

출처 및 근거

ORD 기록
ord-abcfd28db41d491a8c69383a55980740
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09149038B2

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