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Sodium Hydroxide → 2-[2-(4-Methoxyphenyl)ethyl]nicotinic acid

HRID 1581674
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HRID 1581674 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH:10][C:11]2[N:19]=[CH:18][CH:17]=[CH:16][C:12]=2[C:13]([OH:15])=[O:14])=[CH:5][CH:4]=1.[OH-].[Na+]>O.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11]2[N:19]=[CH:18][CH:17]=[CH:16][C:12]=2[C:13]([OH:15])=[O:14])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 688974612-[2-(4-Methoxyphenyl)ethenyl]nicotinic acid

생성물 1

HCID 121253972-[2-(4-Methoxyphenyl)ethyl]nicotinic acid수율 84.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 962Water용매

실험 절차

10% Pd/C (2.21 g, 2.08 mmole) was added to a solution of 2-[2-(4-methoxyphenyl)ethenyl]nicotinic acid (5.31 g, 20.80 mmole) and 1.0 N NaOH (23 mL, 23 mmole) in H2O (81 mL), and the mixture was shaken at RT under H2 (50 psi) on a Parr apparatus. After 4.5 hr, the mixture was filtered through celite®, and the filtrate was acidified to pH 5 with glacial acetic acid. The solid was collected by suction filtration, washed with H2O, and dried in high vacuum at 45° C. to afford the title compound (4.50 g, 84%) as an off-white solid: 1H NMR (400 MHz, DMSO-d6) δ 8.65 (dd. J=4.7, 1.7 Hz, 1H), 8.15 (dd, J=7.8, 1.7 Hz, 1H), 7.35 (dd, J=7.8, 4.7 Hz, 1H), 7.13 (d, J=8.5 Hz, 2H), 6.84 (d, J=8.5 Hz, 2H), 3.71 (s, 3H), 3.25-3.40 (m, 2H), 2.82-2.93 (m, 2H).

후처리

  1. filtrationthe mixture was filtered through celite®
  2. filtrationThe solid was collected by suction filtration
  3. washwashed with H2O
  4. customdried in high vacuum at 45° C.

출처 및 근거

ORD 기록
ord-4b269f0110ae4cdc9322f57a6c488b35
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06730684B1

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