HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641581Generated: November 4, 2026
4-Chlorobenzaldehyde → HCID 86633525, compound
https://huagongshe.com/reaction/1641581
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 12009091 | HCID 12009091 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86633525 | HCID 86633525 | 78% |
Reaction Steps
In dichloromethane (3.0 mL) were dissolved 1-phenylhex-4-yn-1-ol (0.28 mmol) and 4-chlorobenzaldehyde (0.34 mmol) and the solution was cooled to −78° C. before the addition of trimethylsilyltriflate (TMSOTf) (0.86 mmol) thereto. After being stirred for 1 hour at the same temperature, the reaction solution was slowly heated to room temperature over 3 hours. Stirring was further conducted at room temperature for an additional one to two hours in the reaction solution. After the addition of an aqueous NaHCO3 solution, the reaction solution was diluted with diethylether. The organic layer was washed with water and brine, dried over MgSO4, filtered and concentrated. The purification of the concentrate through column chromatography afforded the title compound (Yield 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08115019B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-481bf837d3524dd7919da82127722f06 |
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| Source note | uspto-grants-2012_02 |
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