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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 → HCID 13135248、化合物

HRID 354540
ノート
印刷プレビュー

反応式

HRID 354540 の反応式
[C:1]([C:3]1[C:4]([CH3:13])=[C:5]([C:9]([CH3:12])=[CH:10][CH:11]=1)[C:6](O)=[O:7])#[N:2].B.O.C(=O)([O-])[O-].[K+].[K+]>O1CCCC1>[C:1]([C:3]1[C:4]([CH3:13])=[C:5]([CH2:6][OH:7])[C:9]([CH3:12])=[CH:10][CH:11]=1)#[N:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 6331BoraneHCID 11430Potassium CarbonateHCID 13135247HCID 13135247、化合物

生成物 1

HCID 13135248HCID 13135248、化合物収率 37.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 3-cyano-2,6-dimethylbenzoic acid (8.11 grams, 0.049 mole) in tetrahydrofuran (100 ml) was cooled to 0°. Borane (48.7 grams, 0.049 mole) in tetrahydrofuran was added dropwise over a 20 minute period. The mixture was allowed to come to room temperature, and water was added. Potassium carbonate was added to separate the layers. The aqueous layer was extracted with diethyl ether. The extract was added to the organic phase, which was dried over magnesium sulfate, filtered, and the solvent evaporated to give (3-cyano-2,6-dimethylphenyl)methanol (2.93 grams).

後処理

  1. customto come to room temperature
  2. customto separate the layers
  3. extractionThe aqueous layer was extracted with diethyl ether
  4. additionThe extract was added to the organic phase, which
  5. dry with materialwas dried over magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent evaporated

出典と根拠

ORDレコード
ord-b4710c02690841ae94fc02b6b2f138f5
出典データセット
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04375476

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート