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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 6-bromo-2,2-dimethyl-4H-spiro[chromene-3,3'-oxetan]-4-one | HCID 86724243 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 触媒 | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,3'-oxetane] | HCID 86724242 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08975415B2 |
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| 出典データセット | uspto-grants-2015_03 |
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| ORD ID | ord-bc95b8f70f4a456e9b7a4b1a15e9fdc9 |
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| 出典メモ | uspto-grants-2015_03 |
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