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Acetyl chloride → (5-Methoxy-2-methylphenyl)thiourea

HRID 1753761
ノート
印刷プレビュー

反応式

HRID 1753761 の反応式
[C:1]([S-:3])#[N:2].[K+].C(Cl)(C)=O.[CH3:9][O:10][C:11]1[CH:12]=[CH:13][C:14]([CH3:18])=[C:15]([CH:17]=1)[NH2:16].C([O-])([O-])=O.[K+].[K+]>CC(C)=O.CO.O>[CH3:9][O:10][C:11]1[CH:12]=[CH:13][C:14]([CH3:18])=[C:15]([NH:16][C:1]([NH2:2])=[S:3])[CH:17]=1
参加物反応条件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 6367Acetyl chlorideHCID 11430Potassium CarbonateHCID 995005-Methoxy-o-toluidineHCID 516872Potassium thiocyanate

生成物 1

HCID 3607236(5-Methoxy-2-methylphenyl)thiourea収率 78%

試薬・触媒・溶媒 3

HCID 180Acetone溶媒3 回
HCID 887
Methanol
溶媒
HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

To a solution of KSCN (780 mg, 8.02 mmol) in acetone (10 mL) was added dropwise at room temperature as solution of AcCl (900 μL, 8.02 mmol) in acetone (10 mL). The reaction mixture was stirred for 15 min at 50° C. Then, a solution of 5-methoxy-2-methylaniline (1.0 g, 7.29 mmol) in acetone (10 mL) was added and the reaction mixture was stirred at 50° C. for 15 min. Water was added and the solid was filtered, washed with more water and ether to give a white solid. A solution of the latter with K2CO3 (2.0 g, 14.58 mmol) in MeOH (20 mL) was stirred at room temperature for 3 h. MeOH was removed under reduced pressure and the solid was washed with water and ether to give III-b as a white solid in 78% yield. 1H NMR (300 MHz, DMSO-d6) δ 9.20 (s, 1H), 7.13 (d, J=8.4 Hz, 1H), 6.81 (d, J=2.4 Hz, 1H), 6.75 (dd, J=8.3, 2.6 Hz, 1H), 3.71 (s, 3H), 2.10 (s, 3H).

後処理

  1. stirringthe reaction mixture was stirred at 50° C. for 15 min
  2. filtrationthe solid was filtered
  3. washwashed with more water and ether
  4. customto give a white solid
  5. customMeOH was removed under reduced pressure
  6. washthe solid was washed with water and ether
  7. customto give III-b as a white solid in 78% yield

出典と根拠

ORDレコード
ord-852c2d0d26ee4266979d91a56b73008c
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09168245B2

反応ノート

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