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

Methyl 1-isopropyl-3-oxocyclopentanecarboxylate → 1-Isopropyl-3-oxocyclopentanecarboxylic acid

HRID 1725758
노트
인쇄 미리보기

반응식

HRID 1725758 반응식
[O:1]=[C:2]1[CH2:6][CH2:5][C:4]([CH:11]([CH3:13])[CH3:12])([C:7]([O:9]C)=[O:8])[CH2:3]1>O1CCOCC1.Cl>[O:1]=[C:2]1[CH2:6][CH2:5][C:4]([CH:11]([CH3:13])[CH3:12])([C:7]([OH:9])=[O:8])[CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 18614358Methyl 1-isopropyl-3-oxocyclopentanecarboxylate

생성물 1

HCID 186143931-Isopropyl-3-oxocyclopentanecarboxylic acid

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

반응 조건

온도
0 °C

실험 절차

A solution of methyl 3-oxo-1-isopropylcyclopentanecarboxylate (27 g, 146.6 mmol) in dioxane (300 mL) and conc HCl (100 mL) was heated to reflux overnight. The crude product was extracted into diethyl ether (4×200 mL) and the combined organic extracts were washed with an aqueous solution of sodium hydroxide (5N, 2×150 mL). The combined aqueous extracts were cooled to 0° C. and acidified with conc HCl. The product was extracted with ether (3×200 mL), dried with magnesium sulfate and the solvent was evaporated in vacuo. The weight of the product was 20 g (98%). 1H NMR (500 MHz, CDCl3): 2.81 (d, J=8.54 Hz, 1H), 2.48 (m, 1H), 2.32 (m, 2H), 2.15 (d, J=18.53 Hz, 1H), 2.08 (m, 1H), 1.95 (m, 1H), 1.03 (d, J=6.86 Hz, 3H), 0.96 (d, J=6.87 Hz, 1H).

후처리

  1. temperatureto reflux overnight
  2. extractionThe crude product was extracted into diethyl ether (4×200 mL)
  3. washthe combined organic extracts were washed with an aqueous solution of sodium hydroxide (5N, 2×150 mL)
  4. extractionThe product was extracted with ether (3×200 mL)
  5. dry with materialdried with magnesium sulfate
  6. customthe solvent was evaporated in vacuo

출처 및 근거

ORD 기록
ord-ff137bfcf44f41da9bf2ee3ea1c70439
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07491737B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트