Hydrochloric Acid → 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfinic acid

HRID 584027ノート

反応式

HRID 584027 の反応式
[Cl:1][C:2]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[C:17]([Cl:24])[C:3]=1[O:4][C:5]1[CH:6]=[CH:7][C:8]([O:15][CH3:16])=[C:9]([S:11](Cl)(=[O:13])=[O:12])[CH:10]=1.S([O-])([O-])=O.[Na+].[Na+].C(=O)(O)[O-].[Na+].Cl>O>[Cl:1][C:2]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[C:17]([Cl:24])[C:3]=1[O:4][C:5]1[CH:6]=[CH:7][C:8]([O:15][CH3:16])=[C:9]([S:11]([OH:13])=[O:12])[CH:10]=1

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 24437Sodium SulfiteHCID 516892Sodium BicarbonateHCID 155414425-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfonyl chloride

生成物 1

HCID 223448795-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfinic acid収率 65.7%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

To a solution of 5-(2,6-dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfonyl chloride (4.26 g, 10.3 mmol) in water (40 mL) was added sodium sulfite (3.89 g, 30.9 mmol) and sodium bicarbonate (5.19 g, 61.8 mmol). The resulting mixture was heated to reflux for 2 h and then cooled to RT. The solution was acidified with conc. HCl (5 mL) followed by addition of water (40 mL). The aqueous solution was extracted with EtOAc (5×80 mL). The combined organic extracts were washed with brine (2×50 mL), dried and concentrated to give the title compound of Step B (2.56 g) as a solid. The title product of Step B was used in the next step without purification. MS (APCl−) Calc.: 376.9. Found: 375.8 (M−1).

後処理

  1. temperatureThe resulting mixture was heated
  2. temperatureto reflux for 2 h
  3. extractionThe aqueous solution was extracted with EtOAc (5×80 mL)
  4. washThe combined organic extracts were washed with brine (2×50 mL)
  5. customdried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-477ef20c3e674dc18ddf9629c0e4b906
出典データセット
uspto-grants-2005_08
特許番号
US06924310B2

反応ノート

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