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Hydrochloric Acid → 2-Chloro-6-fluoro-3-(propylsulfonamido)benzoic acid

HRID 2196642
ノート
印刷プレビュー

反応式

HRID 2196642 の反応式
[Cl:1][C:2]1[C:17]([NH:18][S:19]([CH2:22][CH2:23][CH3:24])(=[O:21])=[O:20])=[CH:16][CH:15]=[C:14]([F:25])[C:3]=1[C:4]([O:6]CC1C=CC=CC=1)=[O:5].[OH-].[Ba+2].[OH-].Cl.C(=O)(O)[O-].[Na+]>O1CCOCC1.O>[Cl:1][C:2]1[C:17]([NH:18][S:19]([CH2:22][CH2:23][CH3:24])(=[O:20])=[O:21])=[CH:16][CH:15]=[C:14]([F:25])[C:3]=1[C:4]([OH:6])=[O:5]
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

7

反応物 4

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 6093286Barium hydroxideHCID 66840819Benzyl 2-chloro-6-fluoro-3-(propylsulfonamido)benzoate

生成物 1

HCID 580953612-Chloro-6-fluoro-3-(propylsulfonamido)benzoic acid収率 56.6%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 312751,4-Dioxane溶媒

反応条件

温度
80 °C

実験手順

Benzyl 2-chloro-6-fluoro-3-(propylsulfonamido)benzoate (174.5 mg, 0.4523 mmol) was dissolved in 3:1 dioxane:water (7.5 mL) and treated with barium hydroxide (100.7 mg, 0.5879 mmol). The reaction mixture was heated to 80° C. for 16 hours and then allowed to cool to ambient temperature. The mixture was acidified to a pH of 0 with concentrated HCl. The reaction mixture was allowed to stir for 10 minutes, after which the pH was adjusted to a pH of 4 using saturated sodium bicarbonate. The mixture was extracted with EtOAc (2×). The extracts were washed with water (2×) and brine (1×), dried over sodium sulfate, and concentrated to afford 2-chloro-6-fluoro-3-(propylsulfonamido)benzoic acid (75.7 mg, 0.2560 mmol, 56.6% yield). MS (APCI-neg) m/z=293.9 (M-H).

後処理

  1. temperatureto cool to ambient temperature
  2. extractionThe mixture was extracted with EtOAc (2×)
  3. washThe extracts were washed with water (2×) and brine (1×)
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-3e5c755fa0ba4083ac231edaceca1e6f
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08338452B2

反応ノート

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