Carbon Dioxide → HCID 12230326, 화합물

HRID 855284노트

반응식

HRID 855284 반응식
Br[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8]([CH3:11])=[CH:7]2.[Li]CCCC.[C:17](=[O:19])=[O:18].O>C1COCC1.CCCCCC>[CH3:11][C:8]1[NH:9][C:10]2[C:6]([CH:7]=1)=[CH:5][CH:4]=[CH:3][C:2]=2[C:17]([OH:19])=[O:18]

참가 물질

7

반응물 4

HCID 280Carbon DioxideHCID 962WaterHCID 44130817-Bromo-2-methylindoleHCID 178418339Butyllithium

생성물 1

HCID 12230326HCID 12230326, 화합물수율 31%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8058Hexane용매

반응 조건

온도
2.5 °C

실험 절차

1000 mg of 7-bromo-2-methyl-indole (4.8 mmol) were dissolved in 15 ml THF and 8.9 ml of a 1.6 molar solution of n-BuLi in hexane were added at −78° C. The reaction mixture was then allowed to warm to 0-5° C. and was stirred at this temperature for 30 min. Then it was cooled again to −78° C., dry ice was added and the mixture was allowed to warm to rt. After 15 min at rt it was poured into water and extracted twice with ether. The aqueous phase was then acidified with 1 N HCl solution and extracted several times with DCM. The combined DCM extracts were then dried with magnesium sulfate, filtered and the solvent was evaporated. The remaining residue was triturated with pentane. Final filtration yielded 157 mg (31%) of 2-methyl-1H-indole-7-carboxylic acid as an off-white solid. MS (ISP) 174.3 (M−H)−.

후처리

  1. temperatureThen it was cooled again to −78° C.
  2. temperatureto warm to rt
  3. extractionextracted twice with ether
  4. extractionextracted several times with DCM
  5. dry with materialThe combined DCM extracts were then dried with magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent was evaporated
  8. customThe remaining residue was triturated with pentane
  9. filtrationFinal filtration

출처 및 근거

ORD 기록
ord-9bb3c9e942174166ad9c08e81dbe5e5f
출처 데이터셋
uspto-grants-2007_08
특허 번호
US07259183B2

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