Sulfuric Acid → 2-Amino-3,6-difluorobenzamide

HRID 1467418ノート

反応式

HRID 1467418 の反応式
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].S(=O)(=O)(O)[OH:13].[NH4+].[OH-]>O>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]([NH2:5])=[O:13]

参加物

5

反応物 3

HCID 1118Sulfuric AcidHCID 14923Ammonium Hydroxide2 回HCID 450905912-Amino-3,6-difluorobenzonitrile

生成物 1

HCID 592230322-Amino-3,6-difluorobenzamide

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
70 °C

実験手順

2-Amino-3,6-difluorobenzonitrile (2.3 g, 15 mmol) was added to concentrated sulfuric acid (5 mL) in a 25 mL 2-necked flask equipped with a thermometer with good stirring. The temperature rose to around 40° C. and the mixture became homogeneous. The solution was heated to 70° C. for 2 hours, cooled to room temperature, poured over ice, neutralized with concentrated NH4OH using water and NH4OH to rinse the flask and adding ice as necessary to keep the mixture cold. The separated solid was collected by filtration, washed with water and dried to give 2-amino-3,6-difluorobenzamide, 2.2 g. A second crop of 0.24 g was collected from the cold, concentrated filtrate, 95% overall. M.P. 121-123° C., LC/MS (ESI) m/z 172, 1H NMR (300 MHz, d6-DMSO) δ 7.70 (bs, 1H), 7.63 (bs, 1H), 7.10 (m, 1H), 6.32 (m, 1H), 6.05 (bs, 2H).

後処理

  1. customequipped with a thermometer with good stirring
  2. customrose to around 40° C.
  3. temperaturecooled to room temperature
  4. washto rinse the flask
  5. additionadding ice as necessary
  6. filtrationThe separated solid was collected by filtration
  7. washwashed with water
  8. customdried

出典と根拠

ORDレコード
ord-8068c9cf6a3e43b4a4b8457b2cea027b
出典データセット
uspto-grants-2015_04
特許番号
US09000162B2

反応ノート

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