HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415390Generated: November 2, 2026
Oxalyl chloride → 5-Bromofuran-2-carbonyl chloride
https://huagongshe.com/reaction/2415390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-Bromo-2-furanecarboxylic acid | HCID 68511 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromofuran-2-carbonyl chloride | HCID 2757011 | — |
Reaction Steps
To a solution of 5-bromo-2-furoic acid (2.1 g, 6.856 mmol) in THF (20 mL) was added oxalyl chloride (0.66 mL, 7.541 mmol). 2 drops of DMF were then added to the reaction mixture, with bubbles of CO observed to come out vigorously. Oxalyl chloride ((COCl)2) (0.1 mL) was then added. The reaction mixture was stirred at room temperature for 10 min and at 90° C. for 10 min. Solvent and excess (COCl)2 were taken off under vacuum to yield 5-bromo-furan-2-carbonyl chloride as a pale yellow crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818646B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-e02feec050234453bf06afed686a6cd0 |
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| Source note | uspto-grants-2004_11 |
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