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Water → HCID 20496709, 화합물

HRID 1074443
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HRID 1074443 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15](O)=[O:16])=[CH:6][CH:5]=1)([O-:3])=[O:2].O>O1CCCC1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][OH:16])=[CH:8][CH:9]=1)([O-:3])=[O:2]
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참가 물질

4

반응물 2

HCID 962WaterHCID 204967086-(4-Nitrophenyl)hexanoic acid

생성물 1

HCID 20496709HCID 20496709, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 9.1 g of 6-(4-nitrophenyl)hexanoic acid in 200 ml of dried tetrahydrofuran was added, dropwise, a solution of borane-dimethyl sulfide complex (0.042 mole) in 40 ml of dried tetrahydrofuran. The resulting mixture was stirred at room temperature for 16 hours and then heated at reflux for 1 hour before it was cooled again to room temperature. Water (10 ml) was added, the mixture was stirred for 15 minutes, most of the solvent was removed, and water was added to the residue. The resultant aqueous mixture was extracted with diethyl ether and the extract was washed with aqueous saturated sodium bicarbonate solution, water, and aqueous saturated sodium chloride solution and dried over magnesium sulfate. The solvent was then evaporated to leave 6-(4-nitrophenyl)hexanol as a yellow oil.

후처리

  1. temperatureheated
  2. temperatureat reflux for 1 hour before it
  3. temperaturewas cooled again to room temperature
  4. stirringthe mixture was stirred for 15 minutes, most of the solvent
  5. customwas removed
  6. additionwater was added to the residue
  7. extractionThe resultant aqueous mixture was extracted with diethyl ether
  8. washthe extract was washed with aqueous saturated sodium bicarbonate solution, water, and aqueous saturated sodium chloride solution
  9. dry with materialdried over magnesium sulfate
  10. customThe solvent was then evaporated

출처 및 근거

ORD 기록
ord-558e1882e01947e7a718a141a11336d6
출처 데이터셋
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04391818

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