HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594848Generated: October 25, 2026
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/594848
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-bromo-2,2-dimethyl-4H-spiro[chromene-3,3'-oxetan]-4-one | HCID 86724243 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,3'-oxetane] | HCID 86724242 | 92% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242973B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-a6ed86a4ff334c0aaf3376c939ba6850 |
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| Source note | uspto-grants-2016_01 |
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