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Acetone → Methyl 2-methylazulene-1-carboxylate

HRID 1721461
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반응식

HRID 1721461 반응식
[CH3:1][O:2][C:3]([C:5]1C(=O)O[C:7]2=[CH:11][CH:12]=[CH:13][CH:14]=[CH:15][C:6]=12)=[O:4].[CH3:16]C(C)=O.C(N[CH2:23][CH3:24])C>O>[CH3:1][O:2][C:3]([C:5]1[C:6]2[C:7]([CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)=[CH:16][C:23]=1[CH3:24])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 8021DiethylamineHCID 100816163-(Methoxycarbonyl)-2H-cyclohepta[b]furan-2-one

생성물 1

HCID 11264110Methyl 2-methylazulene-1-carboxylate

시약·촉매·용매 1

HCID 962Water용매

실험 절차

2-Methylazulene was synthesized according to a method described in Japanese Patent Laid-Open Publication No. 207232/1987. Specifically, 19.5 g (0.16 mol) of tropolone was reacted with 40 g (0.21 mol) of p-toluenesulfonic acid chloride in pyridine to give 37.1 g of tosylated tropolone. Then, 20 g (0.15 mol) of dimethylmalonate was reacted with 9.7 g (0.18 mol) of NaOMe in methanol at room temperature for 4 hr to give 14.4 g of 3-methoxycarbonyl-2H-cyclohepta(b) furan-2-one (Compound (2)). Then, 12 g of Compound (2), 200 ml of acetone and 70 ml of diethylamine were added, and the mixture was heated under reflux for 30 hr. Thereafter, H2O was added thereto, and the mixture was extracted with toluene to give 39.2 g of methyl-2-methylazulene carboxylate. Further, 25 ml of phosphoric acid was added, and a reaction was allowed to proceed at 85° to 90° C. for one hr. The reaction mixture was decomposed with water, extracted with benzene and dried to give 6.5 g of 2-methylazulene as an intended product.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 30 hr
  3. extractionthe mixture was extracted with toluene

출처 및 근거

ORD 기록
ord-5c7093494559404f8ca1135715b75507
출처 데이터셋
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05510502

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