HCID 18918301、化合物 → Ethyl 3-(4-hydroxyphenoxy)butyrate

HRID 1290549ノート

反応式

HRID 1290549 の反応式
C([O:8][C:9]1[CH:23]=[CH:22][C:12]([O:13][CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:11][CH:10]=1)C1C=CC=CC=1.[H][H]>C(O)C.[Pd]>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([O:13][CH:14]([CH3:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:22][CH:23]=1

参加物

5

実験手順

To a solution of the product of step i) (4.5 g) in absolute ethanol (200 ml) was added 10% palladium-on-charcoal catalyst (1.2 g) and the resulting suspension hydrogenated at ambient temperature and pressure until uptake of hydrogen ceased. The catalyst was removed by filtration through celite and the filtrate was concentrated in vacuo to give ethyl 3-(4-hydroxyphenoxy)butyrate as a low-melting crystalline solid (3.0 g) NMR (d6DMSO) δ 1.25(3H,t); 1.8-2.0(2H,m); 2.5(2H,t); 3.9(2H,t); 4.1(2H,q); 6.7(4H,m); 8.8)1H,brs); m/e 224 (M)+.

後処理

  1. customhydrogenated at ambient temperature
  2. customThe catalyst was removed by filtration through celite
  3. concentrationthe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-9052a48bb17e4711b0220a3c229babe2
出典データセット
uspto-grants-1998_05
特許番号
US05750754

反応ノート

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