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HCID 57712919, 화합물 → 5-(2,4-Dimethoxyphenyl)pentanoic acid

HRID 1983428
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HRID 1983428 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[CH:5][C:4]=1/[CH:11]=[CH:12]/[CH2:13][CH2:14][C:15]([OH:17])=[O:16]>C(O)(=O)C>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[CH:5][C:4]=1[CH2:11][CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 57712919HCID 57712919, 화합물

생성물 1

HCID 74719765-(2,4-Dimethoxyphenyl)pentanoic acid수율 99%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A 1-L hydrogenation flask was charged with 36.2 g of 5-(2,4-dimethoxyphenyl)-4-pentenoic acid (3a) and 400 ml of glacial acetic acid. The flask was flushed with argon and 2 g of (10% Pd/C) were added to the flask, which was then attached to the hydrogenator. The hydrogenation bottle was evacuated, and charged with hydrogen to 40 to 50 psi. The reaction was run overnight until no further hydrogen was being consumed. The solution was filtered through Cellite (diatomaceous earth). The solvent was evaporated, and the residue dried in vacuo. The yield was 99%. 1H NMR (DMSO-d6) δ: 12.01 (br s, 1H), 6.99 (d, J=8.2 Hz, 1H), 6.49 (d, J=2 Hz, 1H), 6.41 (dd, J1=2 Hz, J2=8.2 Hz, 1H), 3.74 (s, 3H), 3.72 (s, 3H), 2.45 (t, 2H), 2.20 (t, 2H), 1.47 (m, 4H).

후처리

  1. customThe flask was flushed with argon and 2 g of (10% Pd/C)
  2. additionwere added to the flask, which
  3. customThe hydrogenation bottle was evacuated
  4. additioncharged with hydrogen to 40 to 50 psi
  5. customwas being consumed
  6. filtrationThe solution was filtered through Cellite (diatomaceous earth)
  7. customThe solvent was evaporated
  8. customthe residue dried in vacuo

출처 및 근거

ORD 기록
ord-f40e430b32904c9da24c15ad3301a74d
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07541454B2

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