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Sodium Hydroxide → 1-Methyl-4-(2-methoxyethoxy)cyclohexanecarboxylic acid

HRID 2060016
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HRID 2060016 반응식
[CH3:1][C:2]1([C:13]([O:15]CC(C)C)=[O:14])[CH2:7][CH2:6][CH:5]([O:8][CH2:9][CH2:10][O:11][CH3:12])[CH2:4][CH2:3]1.[OH-].[Na+]>O1CCOCC1>[CH3:1][C:2]1([C:13]([OH:15])=[O:14])[CH2:3][CH2:4][CH:5]([O:8][CH2:9][CH2:10][O:11][CH3:12])[CH2:6][CH2:7]1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 59444164Isobutyl 1-methyl-4-(2-methoxyethoxy)cyclohexanecarboxylate

생성물 1

HCID 594440691-Methyl-4-(2-methoxyethoxy)cyclohexanecarboxylic acid

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

A mixture of isobutyl 1-methyl-4-(2-methoxyethoxy)cyclohexanecarboxylate (D68, 27 g, 49.6 mmol), 1,4-dioxane (100 mL) and 3M aqueous sodium hydroxide (100 mL, 300 mmol) was heated at 100° C. for 18 h then cooled and partitioned between water and diethyl ether. The aqueous phase was acidified and extracted with ethyl acetate to give the desired product. Unreacted starting material remained in the ether wash, so the ether was evaporated and the residue dissolved in a mixture of THF (100 mL), methanol (100 mL), and 6M aqueous sodium hydroxide (100 mL) and heated at 65° C. for 18 h then worked up as before to give additional product, which was combined to give 1-methyl-4-(2-methoxyethoxy)cyclohexanecarboxylic acid (9.5 g, 43.9 mmol, 89% yield) as a pale yellow oil.

후처리

  1. temperaturethen cooled
  2. custompartitioned between water and diethyl ether
  3. extractionextracted with ethyl acetate

출처 및 근거

ORD 기록
ord-4b833233410044289241f8c8e27edd28
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278328B2

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