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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713353Generated: October 26, 2026

Trityl chloride → 4-Trityloxy-but-2-en-1-ol

https://huagongshe.com/reaction/1713353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantHexaneHCID 8058—
ReactantTriethylamineHCID 8471—
Reactant2-Butene-1,4-diol, (2Z)-HCID 643790—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Trityloxy-but-2-en-1-olHCID 5411041185.2%

Reaction Steps

Trityl chloride (557 mg; 2 mmol) Et3N (0.306 ml; 2.2 mmol) and DMAP (10 mg; 0.08 mmol) were added to an emulsion of cis-2-buten-1,4-diol (1.76 g; 20 mmol) in DCM (10 ml). The mixture was stirred at room temperature under atmosphere of nitrogen for 24 hours. After such period of time the complete disappearance of trityl chloride was observed by TLC (EtOAC/Hexane 50:50). DCM (20 ml) and water (10 ml) were added to the mixture. The phases were separated and the organic layer was washed with water (10 ml) and brine (10 ml). The solvent was dried over MgSO4 and evaporated under reduced pressure affording a residue (white oil) which was purified by flash chromatography using Hexane/EtOAc 70:30→40:60 as gradient which gave the title product as a colourless oil (563 mg, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795270B2
Source datasetuspto-grants-2010_09
ORD IDord-b7815ae917054dc8a24d52e954c671db
Source noteuspto-grants-2010_09