HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57215Generated: October 25, 2026
1-Bromo-3-chloropropane → 3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylate
https://huagongshe.com/reaction/57215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | 5-(Tetradecyloxy)-2-furoic acid | HCID 115175 | — |
| Reactant | Tetrabutylammonium hydroxide pentahydrate | HCID 86669148 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylate | HCID 66869844 | 69.1% |
Reaction Steps
To a vigorously stirred suspension of 5-(tetradecyloxy)furan-2-carboxylic acid (0.650 g, 2.0 mmol) in 10 mL of N,N-dimethylformamide was added 3-chlorobromopropane (0.618 mL, 6.0 mmol), tetrabutylammonium hydroxide pentahydrate (0.734 g, 4.2 mmol) and sodium iodide (˜20 mg). The suspension appeared to go into solution briefly, and then a very finely dispersed white precipitate was observed. The reaction was allowed to stir for 12 hrs. The suspension was then diluted with EtOAc (100 mL), brine (50 mL) and water (50 mL). The phases were separated and the organic phase was washed with water (50 mL) and brine (50 mL). The organic phase was then dried and concentrated to yield 0.554 g of the title compound. This material was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434718B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-d415c70e93b2457da7ef6543791e7477 |
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| Source note | uspto-grants-2016_09 |
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