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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818680Generated: October 27, 2026

Water → (E)-4-(Trityloxy)but-2-en-1-ol

https://huagongshe.com/reaction/1818680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrityl chlorideHCID 6456—
ReactantEthyl acetate hexaneHCID 21226206—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(E)-4-(Trityloxy)but-2-en-1-olHCID 10882092—

Reaction Steps

A solution of Trityl chloride (500 mg; 1.81 mmol), TEA (0.277 ml; 1.99 mmol) and DMAP (8.8 mg; 0.072 mmol) In dry DCM (5 ml) was added with a syringe to a solution of the diol (10) (800 mg; 9.07 mmol) in DCM (15 ml). The mixture was stirred at room temperature for 1 hour and 30 minutes, then other TrCl, TEA and DMAP (half quantities than before) were added. The reaction was stirred at the same temperature until TLC (Hexane/EtOAc 50:50) showed complete disappearance of Trityl chloride. After 1.5 hours water (20 ml) was added and the reaction was stirred for few minutes, then the phases were separated. The organic layer was washed with water (25 ml) and brine (25 ml). The solvent was dried over MgSO4 and evaporated to afford a crude oil which was purified by flash chromatography using Hexane/EtOAc 50:50 as eluent which gave the title compound as a colourless oil, 637 mg, 71%. Rf: 0.72 in Hexane/EtOAc 50:50 (UV/PMA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601702B2
Source datasetuspto-grants-2009_10
ORD IDord-b2fbc7de4e6e480e8ae11db152852374
Source noteuspto-grants-2009_10