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Hydrochloric Acid → 2-Fluoro-5-oxiranyl-benzenesulfonamide

HRID 990600
ノート
印刷プレビュー

反応式

HRID 990600 の反応式
Br[CH2:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]([F:15])=[C:9]([S:11]([NH2:14])(=[O:13])=[O:12])[CH:10]=1)=[O:4].[BH4-].[Na+].[OH-].[Na+].Cl>CO>[F:15][C:8]1[CH:7]=[CH:6][C:5]([CH:3]2[CH2:2][O:4]2)=[CH:10][C:9]=1[S:11]([NH2:14])(=[O:13])=[O: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 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 118085905-(2-Bromoacetyl)-2-fluorobenzenesulphonamide

生成物 1

HCID 109877122-Fluoro-5-oxiranyl-benzenesulfonamide収率 48.7%

試薬・触媒・溶媒 1

HCID 887Methanol
溶媒

反応条件

温度
0 °C

実験手順

A solution of 0.5 g (1.7 mmol) of 5-bromoacetyl-2-fluoro-benzenesulfonamide V in 20 mL MeOH was cooled to 0° C. NaBH4 26 mg (0.67 mmol) was added and the reaction was stirred at 0° C. for 15 min. 4 mL of 1N NaOH was added and the reaction was stirred at 0° C. for 4 hrs. The reaction was adjusted to pH 6 by addition of dilute HCl. The volatiles were evaporated and the residue dissolved in EtOAc, washed with H2O, dried over Na2SO4 and evaporated. The product was purified by column chromatography on silica gel eluting with CH2Cl2/MeOH::9/1 to give 180 mg of VI (48%); mp 100-103° C.TLC:CH2Cl2/MeOH::9/1 single-spot material Rƒ 0.65.1H-NMR (300 MHz DMSO-D6) δ: (2.82, m, 1H), (3.14, m, 1H), (4.06, m, 1H), (7.40, t, 1H), (7.56, m, 1H), (7.66, m, 3H).

後処理

  1. stirringthe reaction was stirred at 0° C. for 4 hrs
  2. customThe volatiles were evaporated
  3. dissolutionthe residue dissolved in EtOAc
  4. washwashed with H2O
  5. dry with materialdried over Na2SO4
  6. customevaporated
  7. customThe product was purified by column chromatography on silica gel eluting with CH2Cl2/MeOH

出典と根拠

ORDレコード
ord-7d630e878c6b4ee3b761c84695749569
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06461822B2

反応ノート

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