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Potassium Hydroxide → HCID 58236451, 화합물

HRID 1182808
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HRID 1182808 반응식
[OH:1][C:2]1[C:11]([CH:12]([CH3:14])[CH3:13])=[CH:10][C:5]([C:6]([O:8]C)=[O:7])=[C:4]([O:15][CH2:16][O:17][CH3:18])[CH:3]=1.[OH-].[K+]>CO.O>[OH:1][C:2]1[C:11]([CH:12]([CH3:13])[CH3:14])=[CH:10][C:5]([C:6]([OH:8])=[O:7])=[C:4]([O:15][CH2:16][O:17][CH3:18])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 58236469Methyl 4-hydroxy-5-isopropyl-2-(methoxymethyloxy)benzoate

생성물 1

HCID 58236451HCID 58236451, 화합물수율 25%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

The crude methyl 4-hydroxy-5-isopropyl-2-(methoxymethyloxy)benzoate was dissolved in methanol (20 ml) and water (8 ml), aqueous potassium hydroxide (50% w/v, 5 ml) was added and the mixture was stirred and held at reflux for 16 hours. Upon cooling to room temperature the organic solvent was removed in vacuo and the residue acidified by the addition of 2M hydrochloric acid (30 ml). The organic material was extracted with ethyl acetate (2×20 ml) and the combined organic extracts were evaporated in vacuo to afford a yellow oil that was subjected to column chromatography on a Strata-NH2 cartridge. Elution with 2M ammonia in methanol afforded crude 4-hydroxy-5-isopropyl-2-(methoxymethyloxy)benzoic acid (180 mg, 25%) as a pale grey solid that was used without further purification. MS: [M+Na]+ 263.

후처리

  1. temperatureat reflux for 16 hours
  2. customwas removed in vacuo
  3. additionthe residue acidified by the addition of 2M hydrochloric acid (30 ml)
  4. extractionThe organic material was extracted with ethyl acetate (2×20 ml)
  5. customthe combined organic extracts were evaporated in vacuo
  6. customto afford a yellow oil that
  7. washElution with 2M ammonia in methanol

출처 및 근거

ORD 기록
ord-2b6bc231a4614b10a83548f816c329d7
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664218B2

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