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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223326Generated: October 31, 2026

Bromide ion → HCID 59701029, compound

https://huagongshe.com/reaction/2223326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantTetrahydrofuranHCID 8028—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant3-Fluoro-2-methylbenzoic acidHCID 246682—
ReactantCID 53628100HCID 178418400—
ProductHCID 59701029HCID 5970102966%

Reaction Steps

A solution of 3-fluoro-2-methylbenzoic acid (5.0 g, 1.0 equiv) in THF (175 mL) was cooled to −78° C. under an atmosphere of argon. TMEDA (9.86 mL, 2.0 equiv) was added via syringe. s-BuLi (1.4 M in cyclohexane, 49 mL, 2.1 equiv) was added dropwise via addition funnel over 30 min. After stirring for 2.5 hr, the bromide (13.7 g, 1.5 equiv) in THF (25 mL) was added dropwise. Upon completion of the addition, the solution was allowed to stir and warm to room temperature overnight. The reaction was quenched by the addition of water and then diluted with hexanes. The aqueous and organic phases were separated and the organic phase was washed with water. The aqueous phase was acidified to pH=1 with 1N HCl and then extracted with EtOAc. The resulting organic solution was dried over Na2SO4, filtered and concentrated. The residue was rinsed with dichloromethane, filtered, and dried to give the desired product (7.6 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375125B2
Source datasetuspto-grants-2008_05
ORD IDord-602dc42bf7b2409aaec1087569926728
Source noteuspto-grants-2008_05