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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641582Generated: November 2, 2026

Acetaldehyde → HCID 86633526, compound

https://huagongshe.com/reaction/1641582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 12009091HCID 12009091—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 86633526HCID 8663352676%

Reaction Steps

In dichloromethane (3.0 mL) were dissolved 1-phenylhex-4-yn-1-ol (0.28 mmol) and ethanal (0.34 mmol) and the solution was cooled to −78° C. before the addition of trimethylsilyltriflate (TMSOTf) (0.86 mmol) thereto. At the same temperature, the reaction solution was stirred for 1 hour, followed by slow temperature elevation 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 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115019B2
Source datasetuspto-grants-2012_02
ORD IDord-0be12493853e452da90dd841c8fb4aec
Source noteuspto-grants-2012_02