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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Methyl 3-fluoromethyl-5-hydroxymethylbenzoate | HCID 67253567 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 3-azidomethyl-5-fluoromethylbenzoate | HCID 86671517 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633304B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-7cb982ea968b4d24bcc82fc392c3b391 |
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| Source note | uspto-grants-2014_01 |
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