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HRID 573784作成日:2026年10月26日

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 4-Isopropyl-7,7-dimethyl-2',3',5',6',7,8-hexahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]-3,9(6H)-dione

https://huagongshe.com/reaction/573784

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物3-Amino-5,5-dimethyl-2-cyclohexen-1-oneHCID 136680—
反応物L-Ascorbic AcidHCID 54670067—
反応物3-Isobutyryl-1,8-dioxaspiro[4.5]dec-3-en-2-oneHCID 66762855—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物4-Isopropyl-7,7-dimethyl-2',3',5',6',7,8-hexahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]-3,9(6H)-dioneHCID 66762374—

反応条件

温度200 °C

反応手順

3.12 g 3-Isobutyryl-1,8-dioxaspiro[4.5]dec-3-en-2-one and 2.13 g 3-amino-5,5-dimethylcyclohex-2-enone are mixed and heated to 200° C. for 10 minutes under a vacuo of 20 mbar. The mixture is cooled to room temperature, 15 ml ethylacetate are added and the mixture is stirred for 30 minutes. Then 15 ml petrole ether are added and the precipitate is isolated by filtration. The crude product is dissolved in 350 ml dichloromethane, treated with 2.46 g 2,3dichloro-5,6-dicyano-p-benzoquinone and stirred for 18 hours. 2 g Ascorbic acid are added and the mixture is stirred for 10 minutes. The it is washed for three times with water. The organic phase is dried with sodium sulphate and the solvents are evaporated in vacuo. The residue is chromatographed on silica gel (petrole ether/ethylacetate 100:0 to 50:50).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029544B2
出典データセットuspto-grants-2015_05
ORD IDord-c8c75e02cd2941df9fceb65ab2620aad
出典メモuspto-grants-2015_05