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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096628Generated: November 2, 2026

Bromide ion → HCID 58424622, compound

https://huagongshe.com/reaction/2096628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 58423937HCID 58423937—
ProductHCID 58424622HCID 5842462282%

Reaction Steps

To a solution of 6-bromo-4′-t-butylspiro[chroman-2,1′-cyclohexan]-4-one (2.155 g, 6.13 mmol) in anhydrous THF (20 mL) at −78° C. is added a solution of vinylmagnesiun bromide in THF (1 M, 9.2 mL, 9.2 mmol) dropwise within 30 min. The reaction temperature is allowed to warm to rt and stirred for another 2 h. The reaction is chilled to 0° C. and quenched with sat. aq. NH4Cl, and extracted with ethyl acetate (2×40 mL). The combined organic phases are washed with H2O and brine, then dried over Na2SO4, and filtered. The filtrate is concentrated and the residue is purified through flash chromatography on silica gel to afford 6-bromo-4′-tert-butyl-4-vinylspiro[chroman-2,1′-cyclohexan]-4-ol as an oil (1.907 g, 82%). MS ESI +ve m/z 361 (M+H—H2O)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-21b338af851c4dbd8e6b59db7088a59d
Source noteuspto-grants-2013_05