반응식
[CH3:1][C:2]1[O:3][C:4]([CH3:11])=[C:5]([CH3:10])[C:6]=1[C:7](O)=[O:8].S(Cl)([Cl:14])=O>C1(C)C=CC=CC=1>[CH3:1][C:2]1[O:3][C:4]([CH3:11])=[C:5]([CH3:10])[C:6]=1[C:7]([Cl:14])=[O:8]참가 물질
4
실험 절차
2,4,5-Trimethyl-3-furancarbonyl chloride was prepared by refluxing 2,4,5-trimethyl-3-furancarboxylic acid (20.0 g) with thionyl chloride (20 ml) in toluene (75 ml) for 3 hours. The toluene and excess thionyl chloride were removed on a rotary evaporator and the residue distilled (b.p. 95°-97° C. at ca. 12 mm).
후처리
- customThe toluene and excess thionyl chloride were removed on a rotary evaporator
- distillationthe residue distilled (b.p. 95°-97° C. at ca. 12 mm)
출처 및 근거
- ORD 기록
- ord-6e3063683a874e328e6fedbea747620b
- 출처 데이터셋
- uspto-grants-1993_12
- 특허 번호
- US05268389
연결된 노트
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