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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetyl chloride → (5-Methoxy-2-methylphenyl)thiourea

HRID 1753761
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HRID 1753761 반응식
[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
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참가 물질

8

반응물 4

HCID 6367Acetyl chlorideHCID 11430Potassium CarbonateHCID 995005-Methoxy-o-toluidineHCID 516872Potassium thiocyanate

생성물 1

HCID 3607236(5-Methoxy-2-methylphenyl)thiourea수율 78%

시약·촉매·용매 3

HCID 180Acetone용매3회
HCID 887
Methanol
용매
HCID 962Water용매

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온도
50 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-852c2d0d26ee4266979d91a56b73008c
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09168245B2

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