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HRID 4501作成日:2026年10月24日

Dimethylformamide → E-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoic acid chloride

https://huagongshe.com/ja/reaction/4501

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Thionyl ChlorideHCID 24386—
反応物Mycophenolic AcidHCID 446541—
溶媒DichloromethaneHCID 6344—
生成物E-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoic acid chlorideHCID 9997294—

反応手順

E-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoic acid (mycophenolic acid) (32.0 g) was dissolved in dichloromethane (250 ml), followed by the addition of thionyl chloride (25.0 ml) and dimethylformamide (0.3 ml). The reaction mixture was stirred at room temperature for 3 hours, after which the volatile components were removed under vacuum to afford E-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoic acid chloride as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727069
出典データセットuspto-grants-1988_02
ORD IDord-5c4074c08323446d9ace398b44e77c79
出典メモuspto-grants-1988_02