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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → Allyl cyclohexyl ether

HRID 1759675
ノート
印刷プレビュー

反応式

HRID 1759675 の反応式
[CH:1]1([OH:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:8][C:9](C)([O-])[CH3:10].[K+].C(Br)C=C.O>O1CCCC1>[CH:1]1([O:7][CH2:10][CH:9]=[CH2:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 962WaterHCID 7841Allyl bromide2 回HCID 7966CyclohexanolHCID 23665647Potassium tert-butoxideHCID 178418922HCID 178418922、化合物

生成物 1

HCID 11804844Allyl cyclohexyl ether

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

In 870 g of tetrahydrofuran were dissolved 200 g (2 mol) of cyclohexanol and 224 g (2 mol) of potassium t-butoxide. With stirring at room temperature, 242 g (2 mol) of allyl bromide was added dropwise so that the temperature might not exceed 60° C. At the end of addition, the solution was heated at 60° C. on an oil bath and ripened for one hour at the temperature. The solution was allowed to cool down to room temperature, and 11.2 g (0.1 mol) of t-butoxypotassium was added. With stirring at room temperature, 12.1 g (0.1 mol) of allyl bromide was added dropwise. The solution was heated at 60° C. on an oil bath and ripened for one hour at the temperature. The solution was cooled in an ice bath, and 550 g of water was added. The organic layer was collected. The solvent was distilled off in vacuum, yielding 280 g of a crude end product. The product was used in the subsequent reaction without further purification.

後処理

  1. customexceed 60° C
  2. additionAt the end of addition
  3. temperaturethe solution was heated at 60° C. on an oil bath
  4. temperatureto cool down to room temperature
  5. stirringWith stirring at room temperature
  6. temperatureThe solution was heated at 60° C. on an oil bath
  7. waitripened for one hour at the temperature
  8. temperatureThe solution was cooled in an ice bath
  9. customThe organic layer was collected
  10. distillationThe solvent was distilled off in vacuum
  11. customyielding 280 g of a crude end product
  12. customThe product was used in the subsequent reaction without further purification

出典と根拠

ORDレコード
ord-2997996873cd43a4aaa98b171d49d6e4
出典データセット
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06838224B2

反応ノート

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