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Acetate → 1-(2-Hydroxy-4-tetradecylphenyl)ethanone

HRID 34853
ノート
印刷プレビュー

反応式

HRID 34853 の反応式
[CH2:1]([C:15]1[CH:16]=[C:17]([OH:21])[CH:18]=[CH:19][CH:20]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[C:22]([O-])(=[O:24])[CH3:23].[Cl-].[Al+3].[Cl-].[Cl-].Cl>CCOCC>[OH:21][C:17]1[CH:16]=[C:15]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH:20]=[CH:19][C:18]=1[C:22](=[O:24])[CH3:23]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 175AcetateHCID 313Hydrochloric AcidHCID 6451240Aluminum(III) ChlorideHCID 144404953-Tetradecylphenol

生成物 1

HCID 142562101-(2-Hydroxy-4-tetradecylphenyl)ethanone

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

A 20 g portion of 3-tetradecylphenol, acetate was heated at 110° C. and 8.4 g of aluminum chloride was added in portions over a 3 hour period. The mixture was allowed to cool, then diluted with ether, poured onto ice containing 10 ml of concentrated hydrochloric acid and extracted several times with ether. The ether extracts were combined, washed with water, brine and dried. The crude material was chromatographed on silica gel, eluting with hexane:ethyl acetate (50:1), giving 15.8 g of the desired compound, mp 45°-46° C.

後処理

  1. temperatureto cool
  2. extractionextracted several times with ether
  3. washwashed with water, brine
  4. customdried
  5. customThe crude material was chromatographed on silica gel
  6. washeluting with hexane:ethyl acetate (50:1)

出典と根拠

ORDレコード
ord-ef9e87034e254110a8626510cc64c8e6
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04762942

反応ノート

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