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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → 862501-94-8

HRID 555677
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HRID 555677 반응식
[C:1]12([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:8][CH2:7][C:4]([C:9]([O:11]C)=[O:10])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[OH-].[Na+]>CO>[C:1]12([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:2][CH2:3][C:4]([C:9]([OH:11])=[O:10])([CH2:5][CH2:6]1)[CH2:7][CH2:8]2
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 23149682HCID 23149682, 화합물

생성물 1

HCID 23149699862501-94-8수율 73.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1,1-Dimethylethyl methyl bicyclo[2.2.2]octane-1,4-dicarboxylate (495 mg) was dissolved in methanol (5 mL). To this solution, a 2 mol/L aqueous sodium hydroxide solution (0.92 mL) was added and the mixture was stirred at room temperature for 8 hours and then at 50° C. for 2 hours. Methanol in the mixture was evaporated under reduced pressure. Water was added to the resulting residue and the mixture was washed with diethyl ether and was neutralized with 3 mol/L hydrochloric acid. The resulting crystals were filtered, washed with water, and dried under reduced pressure to give 1,1-dimethylethyl hydrogen bicyclo[2.2.2]octane-1,4-dicarboxylate (344 mg).

후처리

  1. waitat 50° C. for 2 hours
  2. customMethanol in the mixture was evaporated under reduced pressure
  3. additionWater was added to the resulting residue
  4. washthe mixture was washed with diethyl ether
  5. filtrationThe resulting crystals were filtered
  6. washwashed with water
  7. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-4f4ac773b7d6430ab5c48f6e88e3463a
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053465B2

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