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4-Toluenesulfonyl chloride → 2,5-Difluoro-3-methoxyphenylacetonitrile

HRID 1108096
ノート
印刷プレビュー

反応式

HRID 1108096 の反応式
[F:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][C:7]([F:12])=[CH:6][C:3]=1[CH2:4]O.C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[CH2:24]([N:26](CC)CC)C.[C-]#N.[Na+]>ClCCl.O.CS(C)=O>[F:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][C:7]([F:12])=[CH:6][C:3]=1[CH2:4][C:24]#[N:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 8929Sodium CyanideHCID 114466172,5-Difluoro-3-methoxybenzyl alcohol

生成物 1

HCID 114353352,5-Difluoro-3-methoxyphenylacetonitrile収率 68.1%

試薬・触媒・溶媒 3

HCID 679Dimethyl Sulfoxide
溶媒
HCID 962Water溶媒2 回
HCID 6344Dichloromethane溶媒

実験手順

To a stirred solution of 2,5-difluoro-3-methoxybenzyl alcohol (8.26 g, 47.4 mmol) in dichloromethane (100 ml) was added p-toluenesulfonyl chloride (9.95 g, 52.2 mmol) and triethylamine (7.30 ml, 52.2 mmol) at room temperature. After 3.5 hr, the mixture was poured into water (200 ml) and extracted with ether (200 ml). The extract was washed with brine (200 ml), dried (magnesium sulfate) and evaporated. To the residue was added DMSO (200 ml) and sodium cyanide (3.48 g, 71 mmol). The resulting mixture was stirred for 2 hr and then poured into water (200 ml) and extracted with ether (300 ml). The extract was washed with water (100 ml), brine (100 ml) and dried over magnesium sulfate. Removal of solvent gave 5.91 g (63%) of the titled compound as a red oil.

後処理

  1. extractionextracted with ether (200 ml)
  2. washThe extract was washed with brine (200 ml)
  3. dry with materialdried (magnesium sulfate)
  4. customevaporated
  5. extractionextracted with ether (300 ml)
  6. washThe extract was washed with water (100 ml), brine (100 ml)
  7. dry with materialdried over magnesium sulfate
  8. customRemoval of solvent

出典と根拠

ORDレコード
ord-eb8491a188fe43cd95e764be17c905ab
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06063928

反応ノート

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