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Acetonitrile → 5-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran

HRID 1850371
ノート
印刷プレビュー

反応式

HRID 1850371 の反応式
[Br:1]N1C(=O)CCC1=O.C(#N)C.[CH3:12][C:13]1([CH3:25])[CH2:17][C:16]2[C:18]([CH3:24])=[CH:19][C:20]([CH3:23])=[C:21]([CH3:22])[C:15]=2[O:14]1>O>[Br:1][C:19]1[C:20]([CH3:23])=[C:21]([CH3:22])[C:15]2[O:14][C:13]([CH3:25])([CH3:12])[CH2:17][C:16]=2[C:18]=1[CH3:24]
参加物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 6342AcetonitrileHCID 67184N-bromobutanimideHCID 117454372,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran

生成物 1

HCID 667609285-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran収率 86%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

N-bromosuccinimide (12.5 g, 70.0 mmol) was added to a solution of acetonitrile (165 mL) containing 2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran (11.1 g, 58.3 mmol) synthesized in Reference Example 3 under ice-cooling condition, and the mixture was warmed to room temperature. After stirring for 5 hours, water was added to the reaction solution. The generated precipitate was collected by filtration and washed with a mixture of acetonitrile/water (1/2). The solid was dried to give 13.5 g of the title compound (yield: 86%).

後処理

  1. customsynthesized in Reference Example 3 under ice-
  2. temperaturecooling condition
  3. filtrationThe generated precipitate was collected by filtration
  4. washwashed with a mixture of acetonitrile/water (1/2)
  5. customThe solid was dried

出典と根拠

ORDレコード
ord-68e6d64275b441dc99a0b8d2cc5cc951
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08957069B2

反応ノート

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