Water → 2-(7-Chlorobenzo[d][1,3]dioxol-5-yl)acetonitrile

HRID 83707ノート

反応式

HRID 83707 の反応式
[Cl:1][C:2]1[C:10]2[O:9][CH2:8][O:7][C:6]=2[CH:5]=[C:4]([CH2:11]Cl)[CH:3]=1.[C-:13]#[N:14].[Na+].O>CS(C)=O>[Cl:1][C:2]1[C:10]2[O:9][CH2:8][O:7][C:6]=2[CH:5]=[C:4]([CH2:11][C:13]#[N:14])[CH:3]=1

参加物

5

反応物 3

HCID 962WaterHCID 8929Sodium CyanideHCID 162270934-Chloro-6-(chloromethyl)-1,3-dioxaindane

生成物 1

HCID 670440102-(7-Chlorobenzo[d][1,3]dioxol-5-yl)acetonitrile収率 59.9%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
40 °C

実験手順

A mixture of 4-chloro-6-(chloromethyl)benzo[d][1,3]dioxole (6.0 g, 29 mmol) and NaCN (1.6 g, 32 mmol) in DMSO (20 mL) was stirred at 40° C. for 1 h and was then poured into water. The mixture was extracted with EtOAc (30 mL×3). The combined organic layers were washed with water and brine, dried over Na2SO4 and evaporated under reduced pressure to afford 2-(7-chlorobenzo[d][1,3]dioxol-5-yl)acetonitrile (3.4 g, 58%). 1H NMR δ 6.81 (s, 1H), 6.71 (s, 1H), 6.07 (s, 2H), 3.64 (s, 2H). 13C-NMR δ149.2, 144.3, 124.4, 122.0, 117.4, 114.3, 107.0, 102.3, 23.1.

後処理

  1. extractionThe mixture was extracted with EtOAc (30 mL×3)
  2. washThe combined organic layers were washed with water and brine
  3. dry with materialdried over Na2SO4
  4. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-f449962f71f04488975b5766caa40f9f
出典データセット
uspto-grants-2014_09
特許番号
US08846753B2

反応ノート

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