Lithium Hydroxide → 4-[[[3-(4-Acetyl-3 hydroxy-2-propylphenoxy)propyl]thio]methyl]1,3 oxathiolane-2,2-dipropanoic acid

HRID 1383134ノート

反応式

HRID 1383134 の反応式
[C:1]([C:4]1[CH:34]=[CH:33][C:7]([O:8][CH2:9][CH2:10][CH2:11][S:12][CH2:13][CH:14]2[CH2:18][O:17][C:16]([CH2:26][CH2:27][C:28]([O:30]CC)=[O:29])([CH2:19][CH2:20][C:21]([O:23]CC)=[O:22])[S:15]2)=[C:6]([CH2:35][CH2:36][CH3:37])[C:5]=1[OH:38])(=[O:3])[CH3:2].[OH-].[Li+]>C(O)C>[C:1]([C:4]1[CH:34]=[CH:33][C:7]([O:8][CH2:9][CH2:10][CH2:11][S:12][CH2:13][CH:14]2[CH2:18][O:17][C:16]([CH2:19][CH2:20][C:21]([OH:23])=[O:22])([CH2:26][CH2:27][C:28]([OH:30])=[O:29])[S:15]2)=[C:6]([CH2:35][CH2:36][CH3:37])[C:5]=1[OH:38])(=[O:3])[CH3:2]

参加物

4

反応物 2

HCID 3939Lithium HydroxideHCID 14405887Diethyl 4-[[[3 (4-acetyl-3-hydroxy-2-propylphenoxy)propyl]thio]methyl]-1,3 oxathiolane-2,2-dipropanoate

生成物 1

HCID 144058884-[[[3-(4-Acetyl-3 hydroxy-2-propylphenoxy)propyl]thio]methyl]1,3 oxathiolane-2,2-dipropanoic acid収率 94.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

The product of Example 2 (3 g, 0.0052 mol) was dissolved in ethanol (50 ml). Aqueous lithium hydroxide solution (2M, 9.2 ml) was added and the reaction solution was stirred at room temperature for 3 hrs. Ethanol was removed using the rotary evaporator and the aqueous residue was acidified to pH2 using aqueous 0.5N sodium bisulfate solution. The oil which separated was extracted with ethyl acetate and the organic layer dried over anhydrous magnesium sulfate. The drying agent was filtered and the filtrate concentrated on the rotary evaporator to give 2.53 g of a colorless oil which was dried at 70° (0.1 mm Hg) for 5 hrs to give the title compound.

後処理

  1. customEthanol was removed
  2. customthe rotary evaporator
  3. customThe oil which separated
  4. extractionwas extracted with ethyl acetate
  5. dry with materialthe organic layer dried over anhydrous magnesium sulfate
  6. filtrationThe drying agent was filtered
  7. concentrationthe filtrate concentrated on the rotary evaporator

出典と根拠

ORDレコード
ord-73b2aa7f110a4bdc8256c225eca1111a
出典データセット
uspto-grants-1989_02
特許番号
US04808729

反応ノート

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