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Methanol → 5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic Acid

HRID 854196
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HRID 854196 반응식
C([O:3][C:4]([C:6]1[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:9]([CH:17]=[O:18])[NH:8][C:7]=1[CH3:19])=[O:5])C.CO.[OH-].[K+]>O>[CH:17]([C:9]1[NH:8][C:7]([CH3:19])=[C:6]([C:4]([OH:5])=[O:3])[C:10]=1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 206047795-formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

생성물 1

HCID 219156195-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic Acid수율 52%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester was dissolved in water (100 mL) and methanol (45 mL) with stirring. Added KOH (2 eq. 1.9 g) and heated in 100° C. After 2.5 h, cooled to room temperature and the remaining ester was removed by extracting into ethyl acetate (200 mL), dried and concentrated. The water layer was acidified to pH=3 using 2N HCl. The white solid was removed by filtration, rinsing with water. The solid was re-concentrated from toluene, triturated with hexanes and dried to afford 2 g (52%) of an off-white solid. 1H NMR (360 MHz, DMSO-d6) δ 12.46 (br s, 1H, CO2H), 11.95 (s, 1H, NH), 9.08 (s, 1H, CHO), 7.36 (s, 5H, ArH), 2.49 (s, 3H, CH3). MS m/z (relative intensity %, ion) found 229 (100, M+); calc. 229.2.

후처리

  1. customthe remaining ester was removed
  2. extractionby extracting into ethyl acetate (200 mL)
  3. customdried
  4. concentrationconcentrated
  5. customThe white solid was removed by filtration
  6. washrinsing with water
  7. concentrationThe solid was re-concentrated from toluene
  8. customtriturated with hexanes
  9. customdried

출처 및 근거

ORD 기록
ord-17ed10cb51dd4b4a9d081bc48b67f66f
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07256189B2

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