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HRID 873702作成日:2026年10月25日

6-bromo-2,2-dimethyl-4H-spiro[chromene-3,3'-oxetan]-4-one → 6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,3'-oxetane]

https://huagongshe.com/reaction/873702

反応式

関与物質

役割名称HCID仕込み量
反応物6-bromo-2,2-dimethyl-4H-spiro[chromene-3,3'-oxetan]-4-oneHCID 86724243—
反応物ButyllithiumHCID 178418339—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒TetrahydrofuranHCID 8028—
生成物6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,3'-oxetane]HCID 8672424292%

反応手順

To a suspension of methyl(triphenyl)phosphonium bromide (8.13 g, 22.3 mmol) in THF (44 mL) was added n-butyllithium (1.65 M in n-hexane, 13.5 mL, 22.3 mmol) in a dry ice-acetone bath under argon atmosphere. The mixture was stirred for 60 minutes in an ice bath. To the mixture was added a mixture of 6-bromo-2,2-dimethyl-4H-spiro[chromene-3,3′-oxetan]-4-one (2.21 g, 7.44 mmol) and THF (11 mL) in an ice bath. The mixture was stirred for 1 hour at ambient temperature. The reaction was quenched by adding water in an ice-water bath. The mixture was partitioned between EtOAc-hexane (1:2) and water. The organic layer was washed with brine, dried over MgSO4, filtered, and the filtrate was evaporated. Purification using silica gel column chromatography (EtOAc-hexane, a linear gradient of EtOAc from 0 to 20%) afforded 6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,3′-oxetane] (2.02 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08975415B2
出典データセットuspto-grants-2015_03
ORD IDord-bc95b8f70f4a456e9b7a4b1a15e9fdc9
出典メモuspto-grants-2015_03