Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473237Generated: October 29, 2026

Carbon tetrabromide → Methyl 3-azidomethyl-5-fluoromethylbenzoate

https://huagongshe.com/reaction/473237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium AzideHCID 33557—
ReactantMethyl 3-fluoromethyl-5-hydroxymethylbenzoateHCID 67253567—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductMethyl 3-azidomethyl-5-fluoromethylbenzoateHCID 8667151753%

Reaction Steps

Methyl 3-fluoromethyl-5-hydroxymethylbenzoate (34) (2.30 g, 11.6 mmol) was dried for 24 hours. Sodium azide (3.77 g, 58.1 mmol), carbon tetrabromide (4.24 g, 12.1 mmol), and triphenylphosphine (3.66 g, 13.9 mmol) were dried for 48 hours. Under Ar atmosphere, these were mixed with triethylamine (3.6 mL), dissolved in DMF (88 mL), and stirred for 93 hours at a room temperature. TLC was used to confirm the progress of the reaction. Then, the mixture was extracted with EtOAc. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to remove the solvent. The residue was purified by neutral silica gel column chromatography (hexane:EtOAc=10:1) to isolate methyl 3-azidomethyl-5-fluoromethylbenzoate (35) (1.37 g, 53%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633304B2
Source datasetuspto-grants-2014_01
ORD IDord-7cb982ea968b4d24bcc82fc392c3b391
Source noteuspto-grants-2014_01