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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497017Generated: October 30, 2026

Benzene, 1-bromo-3-(trifluoromethyl)- → HCID 65916912, compound

https://huagongshe.com/reaction/1497017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 65916912HCID 6591691297%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a round bottom flask was added n-BuLi (3.84 mL, 9.60 mmol) at −78° C. under argon. THF (10 mL) was added followed by addition of 1-bromo-3-(trifluoromethyl)benzene (0.884 mL, 6.40 mmol) in THF (1 mL). The reaction mixture was stirred for 30 minutes at −78° C. A solution of 1,4-dioxaspiro[4.5]decan-8-one (1.00 g, 6.40 mmol) in THF (5 mL) was then added dropwise to the reaction mixture at −70° C. The reaction was stirred for 1 h at −70° C., and then quenched by the addition of 1 N HCl. The reaction mixture was extracted with EtOAc and the organic portions were separated and combined. The organic layer was dried over Na2SO4, filtered, and concentrated to give Intermediate 3A (1.87 g, 6.19 mmol, 97.0% yield). LCMS=325 [M+Na], RT=1.89 minutes (Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199946B2
Source datasetuspto-grants-2015_12
ORD IDord-ec5007e2bcec4a0283810412d317a3ce
Source noteuspto-grants-2015_12