Furfuryl Alcohol → Bis[(furan-2-yl)methyl] pentanedioate

HRID 1633156

반응식

HRID 1633156 반응식
[CH2:1]([OH:7])[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.[C:8]([O:17]C)(=O)[CH2:9][CH2:10][CH2:11][C:12]([O:14][CH3:15])=[O:13].[Na]>CO>[C:12]([O:14][CH2:15][C:5]1[O:6][CH:2]=[CH:3][CH:4]=1)(=[O:13])[CH2:11][CH2:10][CH2:9][C:8]([O:7][CH2:1][C:2]1[O:6][CH:5]=[CH:4][CH:3]=1)=[O:17]

참가 물질

5

반응물 3

HCID 7361Furfuryl AlcoholHCID 14242Dimethyl GlutarateHCID 5360545Sodium

생성물 1

HCID 20274632Bis[(furan-2-yl)methyl] pentanedioate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Furfuryl alcohol (196 parts, 2 moles ) and 160 parts (1 mole) of dimethyl glutarate were mixed, and 0.5-0.75 percent of sodium metal was added. The mixture was heated to a temperature in the range from 101°-115° C. under a nitrogen atmosphere. Methanol was evolved and removed as the reaction progressed. After a period of four hours, a waxy solid was obtained. After washing the product with water, the residue was a liquid which was identified as difurfuryl glutarate by gas chromatography and mass spectrometric analysis.

후처리

  1. temperatureThe mixture was heated to a temperature in the range from 101°-115° C. under a nitrogen atmosphere
  2. customremoved as the reaction
  3. customa waxy solid was obtained
  4. washAfter washing the product with water

출처 및 근거

ORD 기록
ord-32a97204650c4ada863fff53ac301273
출처 데이터셋
uspto-grants-1984_10
특허 번호
US04478962

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