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Water → O-4-bromo-2-methoxyphenyl dimethylcarbamothioate

HRID 13229
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HRID 13229 반응식
[Br:1][C:2]1[CH:3]=C(O)C(OC)=CC=1.N12CCN(CC1)C[CH2:12]2.[CH3:19][N:20]([CH3:24])[C:21](Cl)=[S:22].[OH2:25].CN1[C:31](=[O:32])[CH2:30][CH2:29][CH2:28]1>>[CH3:19][N:20]([CH3:24])[C:21](=[S:22])[O:25][C:30]1[CH:29]=[CH:28][C:2]([Br:1])=[CH:3][C:31]=1[O:32][CH3:12]
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참가 물질

6

반응물 5

HCID 962WaterHCID 9237DabcoHCID 13387N-methyl-2-pyrrolidone2회HCID 27871Dimethylthiocarbamoyl chlorideHCID 1422285-Bromo-2-methoxyphenol

생성물 1

HCID 59339617O-4-bromo-2-methoxyphenyl dimethylcarbamothioate

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온도
50 °C

실험 절차

A mixture of 4-bromoguaiacol (2.05 g, 10.1 mmol) and 1,4-diazabicyclo(2.2.2)octane (1.42 g, 12.6 mmol) in NMP (24 mL) was heated at 50° C. to give a dark-yellow solution. A solution of dimethylthiocarbamoyl chloride (1.37 g, 11.1 mmol) in NMP (2 ml) was added dropwise to the previous solution over 1-2 min. Some precipitated has formed during the addition. The mixture was stirred at 50° C. for 3 h, and then water (25 ml) was added over 5 min at 50° C. The mixture was stirred overnight at r.t., and the precipitate was isolated by filtration, washed twice with water, and dried in vacuo at 50° C. to yield a pale creamed-coloured crystalline solid, 2.11 g (72%).

후처리

  1. customto give a dark-yellow solution
  2. customSome precipitated has formed during the addition
  3. stirringThe mixture was stirred overnight at r.t.
  4. customthe precipitate was isolated by filtration
  5. washwashed twice with water
  6. customdried in vacuo at 50° C.
  7. customto yield a pale creamed-coloured crystalline solid, 2.11 g (72%)

출처 및 근거

ORD 기록
ord-22927637731c442b9632d5b40b43532b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728030B2

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