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Hydrochloric Acid → 3,3-Dimethyl-6-nitroindoline

HRID 238508
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HRID 238508 반응식
[CH3:1][C:2]1([CH3:17])[C:10]2[C:5](=[CH:6][C:7]([N+:11]([O-:13])=[O:12])=[CH:8][CH:9]=2)[N:4](C(=O)C)[CH2:3]1.Cl>CCO>[CH3:1][C:2]1([CH3:17])[C:10]2[C:5](=[CH:6][C:7]([N+:11]([O-:13])=[O:12])=[CH:8][CH:9]=2)[NH:4][CH2:3]1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 161274181-(3,3-Dimethyl-6-nitroindolin-1-yl)ethanone

생성물 1

HCID 219594663,3-Dimethyl-6-nitroindoline

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
70 °C

실험 절차

1-(3,3-Dimethyl-6-nitro-2,3-dihydro-indol-1-yl)ethanone (1.8 g, Step C) was dissolved in EtOH (50 mL), 12N HCl (50 mL) was added and the resulting mixture was heated at 70° C. overnight. After the mixture was concentrated in vacuo, it was partitioned between saturated NaHCO3 solution and EtOAc, the resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo to afford a yellow solid. MS: 193 (M+1). Calc'd. for C10H12N2O2—192.21.

후처리

  1. concentrationAfter the mixture was concentrated in vacuo, it
  2. customwas partitioned between saturated NaHCO3 solution and EtOAc
  3. dry with materialthe resulting organic layer was dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto afford a yellow solid

출처 및 근거

ORD 기록
ord-fb5c69e5fa60499cb5685b37998bf572
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642624B2

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