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

HRID 13229
ノート
印刷プレビュー

反応式

HRID 13229 の反応式
[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]
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

6

反応物 5

HCID 962WaterHCID 9237DabcoHCID 13387N-methyl-2-pyrrolidone2 回HCID 27871Dimethylthiocarbamoyl chlorideHCID 1422285-Bromo-2-methoxyphenol

生成物 1

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

反応条件

温度
50 °C

実験手順

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%).

後処理

  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%)

出典と根拠

ORDレコード
ord-22927637731c442b9632d5b40b43532b
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07728030B2

反応ノート

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