Ammonium Chloride → 4-(2,6,6-Trimethyl-2-cyclohexen-1-ylidene)-butan-2-ol

HRID 596521ノート

反応式

HRID 596521 の反応式
[CH3:1][C:2]1[C:3](=[CH:10][CH:11]=[C:12]([O:14]C(=O)C)[CH3:13])[C:4]([CH3:9])([CH3:8])[CH2:5][CH2:6][CH:7]=1.[BH4-].[Na+].[Cl-].[NH4+]>C(O)C>[CH3:1][C:2]1[C:3](=[CH:10][CH2:11][CH:12]([OH:14])[CH3:13])[C:4]([CH3:8])([CH3:9])[CH2:5][CH2:6][CH:7]=1

参加物

5

反応物 3

HCID 25517Ammonium ChlorideHCID 4311764Sodium borohydrideHCID 534067734-(2,6,6-Trimethylcyclohex-2-en-1-ylidene)but-2-en-2-yl acetate

生成物 1

HCID 536921574-(2,6,6-Trimethyl-2-cyclohexen-1-ylidene)-butan-2-ol収率 107.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

The resulting crude acetoxy compound of formula II (108 g) is dissolved in 400 ml of ethanol (96%) and added dropwise within 10 minutes at 20°-30° C with slight cooling to a suspension of 20 g of sodium borohydride in 600 ml of 96% ethanol. The mixture is then heated until a slight reflux occurs and stirred at this temperature for 15 minutes. The end of the reaction can be detected by a spontaneous colour change from dark-yellow to lemon-yellow. After cooling to room temperature, the cloudy mixture is poured on to saturated ammonium chloride solution/ice and the mixture is extracted with hexane. After the usual washing to neutrality with water and drying over anhydrous sodium sulphate, the solvent is evaporated under a vacuum. There are obtained 96 g of crude 4-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-butan-2-ol (formula III).

後処理

  1. additionadded dropwise within 10 minutes at 20°-30° C
  2. temperatureThe mixture is then heated until
  3. temperaturea slight reflux
  4. customThe end of the reaction
  5. extractionthe mixture is extracted with hexane
  6. washAfter the usual washing to neutrality with water
  7. dry with materialdrying over anhydrous sodium sulphate
  8. customthe solvent is evaporated under a vacuum

出典と根拠

ORDレコード
ord-696b058c424440b3bcd2ac1e3d50c784
出典データセット
uspto-grants-1977_03
特許番号
US04011245

反応ノート

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