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3-[2,4-Bis(methoxymethoxy)phenyl]-2-cyclopenten-1-one → 3-(2,4-Dihydroxyphenyl)-2-cyclopenten-1-one

HRID 2307162
ノート
印刷プレビュー

反応式

HRID 2307162 の反応式
COC[O:4][C:5]1[CH:10]=[C:9]([O:11]COC)[CH:8]=[CH:7][C:6]=1[C:15]1[CH2:19][CH2:18][C:17](=[O:20])[CH:16]=1>CO>[OH:4][C:5]1[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:6]=1[C:15]1[CH2:19][CH2:18][C:17](=[O:20])[CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 223377723-[2,4-Bis(methoxymethoxy)phenyl]-2-cyclopenten-1-one

生成物 1

HCID 223377493-(2,4-Dihydroxyphenyl)-2-cyclopenten-1-one収率 80.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

3-[2,4-Bis(methoxymethoxy)phenyl]-2-cyclopenten-1-one (20 mg) was heated at 50° C. in MeOH (4 ml) containing acidic ion exchange resin (100 mg) for 3 hr. The reaction mixture was filtered and the resin washed with ethyl acetate (20 ml). The filtrate was concentrated in vacuo and the residue purified by flash column chromatography (SiO2, ethyl acetate/petrol, 7:3 v/v) to furnish 3-(2,4-dihydroxyphenyl)-2-cyclopenten-1-one (11 mg, 79%). 3-(2,4-Dihydroxyphenyl)-2-cyclopenten-1-one (6 mg), hydroxylamine hydrochloride (3.3 mg) and triethylamine (6.6 μl) were heated in ethanol (3 ml) under reflux for 3 hr. The reaction mixture was partitioned between ethyl acetate (20 ml) and water (20 ml). The aqueous phase was extracted with ethyl acetate (10 ml), and the combined organic phases were washed with brine (10 ml), dried over magnesium sulfate, and concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO2, ethyl acetate/petrol, 1:1 v/v) to furnish the title compound as a yellow solid and as one major isomer (4 mg, 62%). Data reported for the major isomer: δH (d4-MeOH) 2.74-2.77 (2H, m), 2.96-2.99 (2H, m), 6.34 (1H, dd), 6.38 (1H, d), 6.96 (1H, t), 7.22 (1H, d); m/z (ES−) 204 (M−H)−.

後処理

  1. filtrationThe reaction mixture was filtered
  2. washthe resin washed with ethyl acetate (20 ml)
  3. concentrationThe filtrate was concentrated in vacuo
  4. customthe residue purified by flash column chromatography (SiO2, ethyl acetate/petrol, 7:3 v/v)

出典と根拠

ORDレコード
ord-a7a98dfb577045d2b72efe15cf0379c0
出典データセット
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06828460B2

反応ノート

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