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Sodium Hydroxide → 4-[2-(Indol-2-yl)ethyloxy]benzoic acid

HRID 583659
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HRID 583659 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH2:10][CH2:11][O:12][C:13]1[CH:22]=[CH:21][C:16]([C:17]([O:19]C)=[O:18])=[CH:15][CH:14]=1.[OH-].[Na+]>CO>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH2:10][CH2:11][O:12][C:13]1[CH:22]=[CH:21][C:16]([C:17]([OH:19])=[O:18])=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium Hydroxide3회HCID 18928558Methyl 4[2-(Indol-2-yl)ethyloxy]benzoate

생성물 1

HCID 158507584-[2-(Indol-2-yl)ethyloxy]benzoic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Ester 4-3 (150 mg, 0.51 mmol) and 1N NaOH (1.3 mL, 1.3 mmol) were combined in 10 mL MeOH. After 16 h additional 1N NaOH (5 mL, 5 mmol) was added, and 7 h later, 5 mL more 1N NaOH. After a total of 2 d the mixture was heated at 50° for 1 h, then concentrated, redissolved in H2O, washed with EtOAc, and the pH of the aqueous layer was adjusted to 1 with 20% KHSO4. This was extracted with EtOAc, and this organic layer was washed with brine, dried (MgSO4) and concentrated, providing 4-4 as a gray solid. Rf 0.48 (silica, EtOAc).

후처리

  1. custom7 h
  2. temperatureAfter a total of 2 d the mixture was heated at 50° for 1 h
  3. concentrationconcentrated
  4. dissolutionredissolved in H2O
  5. washwashed with EtOAc
  6. extractionThis was extracted with EtOAc
  7. washthis organic layer was washed with brine
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-34f9d5409df148f4885c167e50e17a35
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05929120

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