Potassium Hydroxide → 2-Methyl-2-(pent-4-yn-1-yl)propanedioicacid

HRID 1197363

반응식

HRID 1197363 반응식
[CH3:1][C:2]([CH2:13][CH2:14][CH2:15][C:16]#[CH:17])([C:8]([O:10]CC)=[O:9])[C:3]([O:5]CC)=[O:4].[OH-].[K+]>C(O)C>[CH3:1][C:2]([CH2:13][CH2:14][CH2:15][C:16]#[CH:17])([C:3]([OH:5])=[O:4])[C:8]([OH:10])=[O:9]

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 19373418Diethyl 2-methyl-2-(pent-4-ynyl)malonate

생성물 1

HCID 193733782-Methyl-2-(pent-4-yn-1-yl)propanedioicacid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of diethyl 2-methyl-2-(pent-4-ynyl)malonate (11 g) and potassium hydroxide (15 g) in 95% ethanol (150 ml) was heated to reflux for 4 hours and then stood at room temperature for 15 hours. The bulk of the solvent was removed in vacuo and the residue was taken up in water. The resulting aqueous phase was washed with dichloromethane before acidification to pH 1 with concentrated hydrochloric acid and further extraction with fresh dichloromethane. These organic extracts were washed with brine before drying over anhydrous magnesium sulphate and evaporation in vacuo. 2-Methyl-2-(pent-4-ynyl)malonic acid was obtained as a pale yellow solid (6.7 g).

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 4 hours
  3. customThe bulk of the solvent was removed in vacuo
  4. washThe resulting aqueous phase was washed with dichloromethane before acidification to pH 1 with concentrated hydrochloric acid and further extraction with fresh dichloromethane
  5. washThese organic extracts were washed with brine
  6. dry with materialbefore drying over anhydrous magnesium sulphate and evaporation in vacuo

출처 및 근거

ORD 기록
ord-290fb43b7c214a4db56f0efde574f2fa
출처 데이터셋
uspto-grants-1992_05
특허 번호
US05116862

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