Sulfuric Acid → 8-Methylsulfonyl-11-(1-hydroxycyclohexyl)-10-undecynoic acid

HRID 263012

反応式

HRID 263012 の反応式
[C:1]([C:3]1([OH:9])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)#[CH:2].C([O:13][C:14](=[O:16])[CH3:15])(=O)C.[S:17](=[O:21])(=O)(O)[OH:18].C(O[C:26]1([C:32]#[CH:33])C[CH2:30][CH2:29][CH2:28][CH2:27]1)(=O)C.[CH3:34]COCC>>[CH3:34][S:17]([CH:32]([CH2:33][C:2]#[C:1][C:3]1([OH:9])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:15][C:14]([OH:13])=[O:16])(=[O:21])=[O:18]

参加物

6

反応物 5

HCID 1118Sulfuric AcidHCID 3283Diethyl EtherHCID 65251-EthynylcyclohexanolHCID 7918Acetic AnhydrideHCID 78903Cyclohexanol, 1-ethynyl-, 1-acetate

生成物 1

HCID 213175308-Methylsulfonyl-11-(1-hydroxycyclohexyl)-10-undecynoic acid

実験手順

1-Ethynylcyclohexan-1-ol(100 g., 0.8 mole) is added dropwise with stirring to a mixture of acetic anhydride (86.7 g., 0.85 mole) and sulfuric acid (0.25 ml.). The temperature of the reaction mixture is kept at 10°-12° C. during the addition by means of an ice bath. The mixture is then stirred without cooling for 1.5 hours. It is then poured into 300 ml. of ice water. The oily product is taken up in ether, washed with water, dilute sodium bicarbonate solution and brine and dried over sodium sulfate. Distillation affords 107 g. (80%) of 1-acetoxy-1-ethynylcyclohexane, b.p. 95°-97° C./15 mm.

後処理

  1. additionThe temperature of the reaction mixture is kept at 10°-12° C. during the addition by means of an ice bath
  2. temperaturewithout cooling for 1.5 hours
  3. additionIt is then poured into 300 ml
  4. washwashed with water, dilute sodium bicarbonate solution and brine
  5. dry with materialdried over sodium sulfate
  6. distillationDistillation
  7. customaffords 107 g

出典と根拠

ORDレコード
ord-6d4234a4f9e34d6e9bf746e354cc576a
出典データセット
uspto-grants-1979_05
特許番号
US04155908

関連ノート

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