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Sulfamic Acid → 3-Methoxy-4-(methoxycarbonyl)benzoic acid

HRID 59316
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HRID 59316 반응식
[CH:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([O:13][CH3:14])[CH:4]=1)=[O:2].S(=O)(=O)([OH:17])N.Cl([O-])=O.[Na+]>CC(C)=O>[CH3:14][O:13][C:5]1[CH:4]=[C:3]([CH:12]=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8])[C:1]([OH:17])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5987Sulfamic AcidHCID 18510332Methyl 4-formyl-2-methoxybenzoateHCID 23668197Sodium Chlorite

생성물 1

HCID 123983053-Methoxy-4-(methoxycarbonyl)benzoic acid수율 123.1%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a cold solution of methyl 4-formyl-2-methoxybenzoate (6.0 g, 7.73 mmol) in acetone (50 mL) was added aqueous sulphamic acid solution (4.5 g, 11.59 mmol) and aqueous sodium chlorite solution (4.04 g, 11.59 mmol) at 0-5° C. The reaction mixture was stirred at RT for 3-4 h. Excess of solvent was removed under vacuum. The obtained residue was diluted with water and basified with saturated sodium bicarbonate solution. The aqueous layer was washed with diethyl ether to remove organic impurities and the obtained aqueous layer was again acidified with conc. HCl. The solid obtained was filtered and suck dried to afford 2.00 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 3.80 (s, 3H), 3.87 (s, 3H), 7.55-7.59 (m, 2H), 7.70 (d, J=7.8 Hz, 1H), 13.37 (s, 1H); MS (m/z): 210.97 (M+H)+.

후처리

  1. customExcess of solvent was removed under vacuum
  2. additionThe obtained residue was diluted with water and basified with saturated sodium bicarbonate solution
  3. washThe aqueous layer was washed with diethyl ether
  4. customto remove organic impurities
  5. customThe solid obtained
  6. filtrationwas filtered
  7. customsuck dried

출처 및 근거

ORD 기록
ord-a1f357554fb7434abb9dc88ac3d07520
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09439890B2

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