p-Toluenesulfonic acid → 2,3,4,5-Tetramethylfuran

HRID 723657노트

반응식

HRID 723657 반응식
[CH3:1][CH:2]([CH:6]([CH3:10])[C:7](=[O:9])[CH3:8])[C:3](=O)[CH3:4].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1C=CC=CC=1>[CH3:4][C:3]1[O:9][C:7]([CH3:8])=[C:6]([CH3:10])[C:2]=1[CH3:1]

참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 328513,4-Dimethylhexane-2,5-dione

생성물 1

HCID 1391982,3,4,5-Tetramethylfuran수율 19.4%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A solution of 3,4-dimethylhexane-2,5-dione (3.00 g, 21.1 mmol) and p-toluenesulfonic acid (401 mg, 2.11 mmol) in benzene (30 mL) was heated to reflux in a Dean-Stark trap overnight. The reaction mixture was distilled at atmospheric pressure to remove the excess benzene. The remaining mixture was transferred to a smaller flask and distilled at atmospheric pressure. The fraction that came over between 80–100° C. was collected to give 509 mg (19%) of compound 219A as a light yellow oil.

후처리

  1. temperatureto reflux in a Dean-Stark trap overnight
  2. distillationThe reaction mixture was distilled at atmospheric pressure
  3. customto remove the excess benzene
  4. customThe remaining mixture was transferred to a smaller flask
  5. distillationdistilled at atmospheric pressure
  6. customcame over between 80–100° C.
  7. customwas collected

출처 및 근거

ORD 기록
ord-62e8ac59efc64eb3a20d463bd21499db
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07141578B2

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