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2-Amino-4-Bromophenol → 5-Bromo-1,3-benzoxazole-2-thiol

HRID 1815754
ノート
印刷プレビュー

反応式

HRID 1815754 の反応式
O(CC)[C:2]([S-])=[S:3].[K+].[NH2:8][C:9]1[CH:14]=[C:13]([Br:15])[CH:12]=[CH:11][C:10]=1[OH:16]>CCO>[Br:15][C:13]1[CH:12]=[CH:11][C:10]2[O:16][C:2](=[S:3])[NH:8][C:9]=2[CH:14]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 3518402-Amino-4-BromophenolHCID 2735045Potassium ethylxanthate

生成物 1

HCID 106331975-Bromo-1,3-benzoxazole-2-thiol収率 90.3%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Potassium ethyl xanthate (416 mg, 2.60 mmol) was added to a solution of 2-amino-4-bromophenol (244 mg, 1.30 mmol) in EtOH (3.24 mL). The reaction mixture was heated at reflux for 4 h. Upon cooling to RT the mixture was concentrated and the resulting residue was dissolved in water. Acetic acid was added until pH=5 and a white solid precipitated from the solution. The solid was filtered, washed with water and dried to afford 270 mg (90%) of a tan powder which was used without further purification: 1H NMR (d6-DMSO, 400 MHz) δ 14.02 (s, 1H), 7.47-7.38 (m, 3H); 13C (d6-DMSO, 400 MHz) δ 181.4, 148.1, 133.7, 127.1, 117.8,118.8, 112.2; MS (Cl) m/z 229.8 (M−1); HPLC retention time=4.34 min.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 4 h
  3. concentrationwas concentrated
  4. dissolutionthe resulting residue was dissolved in water
  5. additionAcetic acid was added until pH=5
  6. customa white solid precipitated from the solution
  7. filtrationThe solid was filtered
  8. washwashed with water
  9. customdried

出典と根拠

ORDレコード
ord-b88e3cf1f0064034acc6b49652da4813
出典データセット
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06881734B2

反応ノート

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