HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629186Generated: October 30, 2026
Phosphorus oxychloride → HCID 104367310, compound
https://huagongshe.com/reaction/629186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 118222843 | HCID 118222843 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 104367310 | HCID 104367310 | 39.1% |
Reaction Steps
To 8 mL dimethylformamide at room temperature was added phosphorous oxychloride (4.0 mL, 43.33 mmol) dropwise. After stirring for 10 minutes at room temperature, 2-(3,3,3-trifluoropropoxyl)thiophene (1.70 g, 8.67 mmol) as a solution in 8 mL dimethylformamide. The resulting solution was heated to 100° C. for 15 minutes. After cooling to room temperature, the reaction mixture was poured into 100 mL of ice-water and stirred vigorously for 5 minutes. Sodium bicarbonate (11 g) was added carefully and the mixture stirred until homogeneous. Organics were extracted with ether (3×100 mL), washed with water (3×50 mL), brine (50 mL), dried over magnesium sulfate, filtered and concentrated. The crude residue was subjected to chromatography on silica gel with gradient elution (0-20% ethyl acetate in hexanes) to give 5-(3,3,3-trifluoropropoxyl)thiophene-2-carbaldehyde (761 mg, 39%) as an off-white solid. Used without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315495B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-f1ac0715e6d34eca90bbe66664fc3622 |
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| Source note | uspto-grants-2016_04 |
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