Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374215Generated: November 1, 2026

Trityl chloride → HCID 15127968, compound

https://huagongshe.com/reaction/2374215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant1,2-ButanediolHCID 11429—
SolventPyridineHCID 1049—
SolventWater ethylacetateHCID 22728543—
ProductHCID 15127968HCID 1512796836.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1,2-butandiol (2 g) in anh. pyridine (15 mL) was added triphenylmethyl chloride (8 g). The dark reaction mixture was heated at 100° C. for 8 hr and stirred at r.t. for 18 hr. The mixture was then poured in EtOAc/H2O, the phases were separated and the organic layer was washed with sat. aq. NaCl and dried over Na2SO4. The solids were filtered and the solvent evaporated. The residual pyiridine was eliminated by filtration through a pad of silica gel (cHex/EtOAc 8:2). The solvent was evaporated and the residue was purified by flash chromatography (silica gel, cHex/EtOAc 95:5) to give the title compound as a yellow oil (2.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462622B2
Source datasetuspto-grants-2008_12
ORD IDord-9677cb77e6f64ba8b993f32568088aef
Source noteuspto-grants-2008_12