홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Potassium Hydroxide → 4,5-dimethyl-3,6-dihydro-2H-pyran-2,2-dicarboxylic acid

HRID 2396119
노트
인쇄 미리보기

반응식

HRID 2396119 반응식
[CH3:1][C:2]1[CH2:3][C:4]([C:14]([O:16]CC)=[O:15])([C:9]([O:11]CC)=[O:10])[O:5][CH2:6][C:7]=1[CH3:8].[OH-].[K+]>O1CCCC1>[CH3:1][C:2]1[CH2:3][C:4]([C:14]([OH:16])=[O:15])([C:9]([OH:11])=[O:10])[O:5][CH2:6][C:7]=1[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 109561712H-Pyran-2,2-dicarboxylic acid, 3,6-dihydro-4,5-dimethyl-, diethyl ester

생성물 1

HCID 189882674,5-dimethyl-3,6-dihydro-2H-pyran-2,2-dicarboxylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Part B. A solution of the ester compound prepared in Part A above (9.63 g, 37.6 mmol) in tetrahydrofuran (150 mL) was treated with an aqueous solution of potassium hydroxide (150 mL, 10N, 1.5 mol), and stirred vigorously at ambient temperature for 48 hours. The solid salt was collected by filtration, and neutralized by dissolving into 1N aqueous hydrochloric acid (200 mL). This was extracted with ethyl acetate (2×200 mL), and the extracts were combined, dried over anhydrous sodium sulfate, filtered and evaporated to afford the product, 3,6-dihydro-4,5-dimethyl-2H-pyran-2,2-dicarboxylic acid, as a waxy solid (7.46 g, 37.3 mmol, 99%). 1H NMR (CDCl3): δ 4.16 (2H, br s); 2.57 (2H, br s); 1.68 (3H, br s); 1.51 (3H, br s). Mass spectrum (NH3 -CI/DDIP): no M+H+ observed.

후처리

  1. filtrationThe solid salt was collected by filtration
  2. dissolutionby dissolving into 1N aqueous hydrochloric acid (200 mL)
  3. extractionThis was extracted with ethyl acetate (2×200 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. customevaporated

출처 및 근거

ORD 기록
ord-69c4f29c16244b26a454c4c63c325c26
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05491152

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트