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HRID 69473作成日:2026年10月25日

Formaldehyde → 6-Methoxy-3,4-dihydro-1H-2-benzopyran-1-one

https://huagongshe.com/reaction/69473

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物DiisopropylamineHCID 7912—
反応物4-Methoxy-2-methylbenzoic acidHCID 597216—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物6-Methoxy-3,4-dihydro-1H-2-benzopyran-1-oneHCID 12401182—

反応手順

A 1.6M solution of n-butyllithium in hexane (145.9 mL) was added dropwise at −78° C. to a solution of diisopropylamine (33.5 mL) in dry THF (190 mL). Then the reaction mixture was warmed to room temperature for 5 min, and then cooled again to −78° C., and a solution of 4-methoxy-2-methylbenzoic acid in dry THF (210 mL) was added dropwise. After stirring at this temperature for 10 min, paraformaldehyde (7 g) was added. Then the reaction mixture was allowed to return to room temperature and it was stirred at this temperature for 4 h. Water was added to the reaction mixture, then the THF was removed in vacuum and then the aqueous phase was extracted with diethyl ether. The aqueous phase was acidified with conc. HCl, the precipitate obtained was filtered off and washed with water several times. In this way the product was obtained with molecular weight 178.06 (C10H10O3); MS (ESI): 179 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822495B2
出典データセットuspto-grants-2014_09
ORD IDord-7fc365ab56c64ed2a4187612a70af1c8
出典メモuspto-grants-2014_09