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Water → HCID 20496709、化合物

HRID 1074443
ノート
印刷プレビュー

反応式

HRID 1074443 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 20496709HCID 20496709、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-558e1882e01947e7a718a141a11336d6
出典データセット
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04391818

反応ノート

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