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Hydrochloric Acid → 6-Methoxy-1-methyl-1-trifluoromethylisochroman

HRID 1978899
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HRID 1978899 반응식
[F:1][C:2]([F:24])([F:23])[C:3]([C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[CH:8][C:7]=1[CH2:14][CH2:15][O:16]C1CCCCO1)(O)[CH3:4].Cl>O>[CH3:13][O:12][C:9]1[CH:8]=[C:7]2[C:6](=[CH:11][CH:10]=1)[C:3]([CH3:4])([C:2]([F:1])([F:23])[F:24])[O:16][CH2:15][CH2:14]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 21202090HCID 21202090, 화합물

생성물 1

HCID 102205196-Methoxy-1-methyl-1-trifluoromethylisochroman수율 138.4%

시약·촉매·용매 1

HCID 962Water용매

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온도
120 °C

실험 절차

A mixture of 1,1,1-Trifluoro-2-(4-methoxy-2-(2-(tetrahydropyran-2-yloxy)ethyl)phenyl)propan-2-ol (470 mg, 1.35 mmol) and conc. hydrochloric acid (4 ml) was stirred at 120° C. for 3 hr. After cooling, the reaction mixture was diluted with water, and the aqueous layer was extracted with dichloromethane. The organic extracts were dried over magnesium sulfate, and concentrated to give the title compound as a brown oil (460 mg). This was used without further purification.

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후처리

  1. temperatureAfter cooling
  2. extractionthe aqueous layer was extracted with dichloromethane
  3. dry with materialThe organic extracts were dried over magnesium sulfate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c2342268f838460fb3c3f5fb226afba5
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06239147B1

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