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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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Tetrahydrofuran → 22625-86-1

HRID 1153688
ノート
印刷プレビュー

反応式

HRID 1153688 の反応式
O1CCC[CH2:2]1.C[Mg]Br.[C:9]([CH:12]1[CH2:17][C:16]([CH3:18])=[CH:15][CH2:14][CH2:13]1)(=[O:11])[CH3:10]>C(OCC)C>[CH3:10][C:9]([CH3:2])([CH:12]1[CH2:13][CH2:14][CH:15]=[C:16]([CH3:18])[CH2:17]1)[OH:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8028Tetrahydrofuran2 回HCID 125634641-(3-Methylcyclohex-3-en-1-yl)ethan-1-oneHCID 178418573HCID 178418573、化合物

生成物 1

HCID 1285024522625-86-1

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
-20 °C

実験手順

To 90 ml of dry tetrahydrofuran maintained in an inert atmosphere at -60° C. was added 45.3 ml of a 3.0M solution of methylmagnesium bromide in diethyl ether followed by dropwise addition of 15.6 g of 5-acetyl-1-methylcyclohexene in a solution of 50 ml dry tetrahydrofuran. The reaction mixture was warmed to -20° C. and stirred for two hours. The resulting reaction mixture was poured into 150 ml of chilled, saturated ammonium chloride solution and extracted three times with 300 ml portions of diethyl ether. The combined extracts were washed successively with 300 ml of water and 300 ml of saturated sodium chloride, dried (MgSO4) and concentrated in vacuo to leave 17.1 g of a pale yellow oil. Distillation of the oil gave 10.7 g of the desired product as a colorless oil, b.p. 63°-65° C. (0.65 mm).

後処理

  1. customThe resulting reaction mixture
  2. additionwas poured into 150 ml
  3. temperatureof chilled
  4. extractionsaturated ammonium chloride solution and extracted three times with 300 ml portions of diethyl ether
  5. washThe combined extracts were washed successively with 300 ml of water and 300 ml of saturated sodium chloride
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-d6b1ee314ee64a5c9efcb4c03337bda5
出典データセット
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04486219

反応ノート

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