Sulfamic Acid → 5-Methoxy-2-nitrobenzoic acid

HRID 440555

반응식

HRID 440555 반응식
S(=O)(=O)(O)N.[CH3:6][O:7][C:8]1[CH:9]=[CH:10][C:11]([N+:16]([O-:18])=[O:17])=[C:12]([CH:15]=1)[CH:13]=[O:14].CC(C)=[O:21].O.Cl([O-])=O.[Na+]>O>[CH3:6][O:7][C:8]1[CH:9]=[CH:10][C:11]([N+:16]([O-:18])=[O:17])=[C:12]([CH:15]=1)[C:13]([OH:21])=[O:14]

참가 물질

6

반응물 4

HCID 5987Sulfamic AcidHCID 2303715-Methoxy-2-nitrobenzaldehydeHCID 18366337Propan-2-one--water (1/1)HCID 23668197Sodium Chlorite

생성물 1

HCID 3392095-Methoxy-2-nitrobenzoic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Sulfamic acid (15.73 g, 0.162 mol) is added to a solution of 5-methoxy-2-nitrobezaldehyde (19.6 g, 0.108 mol) in an acetone/water (1:1) mixture. Sodium chlorite (18.31 g, 80% real, 0.162 mol) is then added to the reaction mixture at a rate which maintains the reaction mixture temperature below 40° C. The resultant reaction mixture is stirred at room temperature for 24 hours and poured into water. The aqueous mixture is extracted with ethyl acetate. The organic extracts are combined, washed sequentially with 2N hydrochloric acid and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title product as a yellow solid.

후처리

  1. customthe reaction mixture temperature below 40° C
  2. customThe resultant reaction mixture
  3. extractionThe aqueous mixture is extracted with ethyl acetate
  4. washwashed sequentially with 2N hydrochloric acid and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-fe3a904c9bd64944ba14beadcb52ad44
출처 데이터셋
uspto-grants-1996_05
특허 번호
US05519133

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