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Hydrochloric Acid → Methyl 4-[5-(formylmethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate

HRID 2248776
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HRID 2248776 반응식
C[O:2][CH:3](OC)[CH2:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH2:14][CH2:15][CH3:16])[CH:9]=[C:8]2[CH2:17][C:18]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][C:19]=1[O:28][CH3:29].Cl>O1CCCC1>[CH:3]([CH2:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH2:14][CH2:15][CH3:16])[CH:9]=[C:8]2[CH2:17][C:18]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][C:19]=1[O:28][CH3:29])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 19995020HCID 19995020, 화합물

생성물 1

HCID 19994986Methyl 4-[5-(formylmethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of methyl 4-[5-(2,2-dimethoxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.46 g) in tetrahydrofuran (7 ml) and b 1M hydrochloric acid (3.6 ml) was stirred at ambient temperature for 11 h, under a nitrogen atmosphere. The mixture was poured onto water, extracted with ethyl acetate (twice), and the extract washed with water (twice), brine, and then dried (MgSO4). The solvent was evaporated to give a dark oil which was used in the next step without further purification.

후처리

  1. additionThe mixture was poured onto water
  2. extractionextracted with ethyl acetate (twice), and the extract
  3. washwashed with water (twice), brine
  4. dry with materialdried (MgSO4)
  5. customThe solvent was evaporated
  6. customto give a dark oil which
  7. customwas used in the next step without further purification

출처 및 근거

ORD 기록
ord-57f97e53e3f847eb9370a42b701a2b47
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05041460

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