1,2-Dibromoethane → 2,3-Dihydro-1,4-benzoxathiin-6-ol

HRID 1246621

反応式

HRID 1246621 の反応式
Br[CH2:2][CH2:3]Br.C([O-])([O-])=O.[K+].[K+].[SH:11][C:12]1[CH:17]=[C:16]([OH:18])[CH:15]=[CH:14][C:13]=1[OH:19]>CC(C)=O>[O:19]1[C:13]2[CH:14]=[CH:15][C:16]([OH:18])=[CH:17][C:12]=2[S:11][CH2:3][CH2:2]1

参加物

5

反応物 3

HCID 78391,2-DibromoethaneHCID 11430Potassium CarbonateHCID 27361672-Mercaptobenzene-1,4-diol

生成物 1

HCID 125159102,3-Dihydro-1,4-benzoxathiin-6-ol収率 55.2%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

実験手順

1,2-Dibromoethane (2.3 mL, 26.7 mmol) and K2CO3 (8.21 g, 59.4 mmol) were slurried in acetone (250 mL) and a solution of 2-sulfanyl-1,4-benzenediol (prepared according to J. Org. Chem. 1990, 55, 2736) (4.22 g, 29.7 mmol) in acetone (50 mL) was added over 4 h to the stirred mixture. Once the addition was complete stirring was continued for a further 10 h before the solvent was removed in vacuo. The residue was partitioned between water (50 mL) and EtOAc (50 mL), the aqueous layer was extracted with EtOAc (50 mL) and the combined organic layers were dried (MgSO4) and evaporated. Purification of the residue by column chromatography [SiO2; 9:1 (pentane/EtOAc)] gave the title compound (2.48 g, 55%) as a pale orange oil; δH (CDCl3, 400 MHz) 3.08 (2H, m), 4.31 (2H, m), 4.44 (1H, s), 6.42 (1H, d), 6.49 (1H, s), 6.66 (1H, d); MS m/z (ES−) 167 (M−H+).

後処理

  1. additionOnce the addition
  2. customwas removed in vacuo
  3. customThe residue was partitioned between water (50 mL) and EtOAc (50 mL)
  4. extractionthe aqueous layer was extracted with EtOAc (50 mL)
  5. dry with materialthe combined organic layers were dried (MgSO4)
  6. customevaporated
  7. customPurification of the residue by column chromatography [SiO2; 9:1 (pentane/EtOAc)]

出典と根拠

ORDレコード
ord-31422edad81740f2b974eb9bb032f709
出典データセット
uspto-grants-2006_10
特許番号
US07129234B2

関連ノート

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