反応式
[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([C:12]([OH:14])=O)[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].S(Cl)([Cl:17])=O>>[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([C:12]([Cl:17])=[O:14])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5]参加物
3
実験手順
5.58 g Of trans-4-pentylcyclohexylcarboxylic acid was heated with 20 ml of thionyl chloride under reflux conditions. After the reaction was completed, the excess of thionyl chloride was removed completely under reduced pressure and the product residue obtained was distilled under reduced pressure. Trans-4-pentylcyclohexylcarbonyl chloride having a boiling point of 103° to 105° C./0.5 mmHg was obtained.
後処理
- customthe excess of thionyl chloride was removed completely under reduced pressure
- customthe product residue obtained
- distillationwas distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-a6066b6dbaaa4fe79ddd37f85dbd565e
- 出典データセット
- uspto-grants-1985_05
- 特許番号
- US04518226
関連ノート
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