Sodium Hydroxide → 4-(2'-Methoxyphenyl)-3-phenylbutyric acid

HRID 982090

反応式

HRID 982090 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH:10]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[CH2:11][C:12]([O:14]CC)=[O:13].[OH-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH:10]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[CH2:11][C:12]([OH:14])=[O:13]

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 20069054Ethyl 4-(2'-methoxyphenyl)-3-phenylbutyrate

生成物 1

HCID 122124054-(2'-Methoxyphenyl)-3-phenylbutyric acid収率 99.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Ethyl 4-(2'-methoxyphenyl)-3-phenylbutyrate (5.7 g, 19 mmol), from Step 3, was dissolved in 25 mL of methanol and 14 mL of 50% aqueous sodium hydroxide solution was added in one portion. The reaction mixture was stirred at ambient temperature for 18 h. The reaction mixture was concentrated and the residue was partitioned between 100 mL of diethyl ether and 100 mL of water. The layers were separated and the aqueous layer was adjusted to pH 6 with 6M aqueous hydrochloric acid solution and extracted with 3×100 mL of diethyl ether. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give 5.1 g (99% yield) of the title compound as a colorless oil. The 1H NMR spectrum was identical to the spectrum reported for the product of Step 5 of Method A, Example 1.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. customthe residue was partitioned between 100 mL of diethyl ether and 100 mL of water
  3. customThe layers were separated
  4. extractionextracted with 3×100 mL of diethyl ether
  5. washwashed with brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-5f25aa7b1c014343877a6b6afeac12ab
出典データセット
uspto-grants-1991_02
特許番号
US04994486

関連ノート

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