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Water → 5-Trifluoromethyl-indan-2-yl-methanol

HRID 1993878
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인쇄 미리보기

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HRID 1993878 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([C:12](O)=[O:13])[CH2:6]2.B.O>C1COCC1>[F:1][C:2]([F:15])([F:16])[C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([CH2:12][OH:13])[CH2:6]2
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참가 물질

5

반응물 3

HCID 962WaterHCID 6331BoraneHCID 668775351H-Indene-2-carboxylic acid, 2,3-dihydro-5-(trifluoromethyl)-

생성물 1

HCID 668775125-Trifluoromethyl-indan-2-yl-methanol수율 101.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
0 °C

실험 절차

The above 5-trifluoromethyl-indan-2-carboxylic acid (1.03 g, 4.47 mmol) was dissolved in THF (25 mL) and cooled to 0° C. To this solution was added a solution of borane in THF (1M, 6.5 mL). The mixture was warmed to room temperature and stirred for 1 hr. The mixture was treated with water (5 mL) and solvents were evaporated. The residue was extracted with ether and hydrochloric acid (1M). The organic phase was washed with brine and sodium bicarbonate solution. The ether solution was dried and solvents were evaporated to give oily material as 5-trifluoromethyl-indan-2-yl-methanol (0.98 g).

후처리

  1. temperatureThe mixture was warmed to room temperature
  2. customwere evaporated
  3. extractionThe residue was extracted with ether and hydrochloric acid (1M)
  4. washThe organic phase was washed with brine and sodium bicarbonate solution
  5. dry with materialThe ether solution was dried
  6. customsolvents were evaporated

출처 및 근거

ORD 기록
ord-fdad3ff1ca1b4aeab707bd15f25a1d48
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07652053B2

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