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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402534Generated: November 1, 2026

Trityl chloride → 2-triphenylmethoxymethyl-2-propen-1-ol

https://huagongshe.com/reaction/2402534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediol, 2-methylene-HCID 77048—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-triphenylmethoxymethyl-2-propen-1-olHCID 1116332662%

Reaction Steps

To a solution of trityl chloride (4.05 g; 14.3 mmol) and 2-methylenepropane-1,3-diol (1.20 mL; 14.3 mmol) in dry CH2Cl2 (20 mL) was added triethylamine (4.0 mL; 28.5 mmol) slowly at room temperature. The reaction was stirred at room temperature for 1 h and then ethyl acetate (100 mL) and saturated aqueous NaHCO3 (30 mL) were added. The organic layer was separated and washed by saturated aqueous NaHCO3 and NaCl respectively, and dried over anhydrous Na2SO4. After evaporation of the solvent, the residue was purified by flash column chromatography over silica gel using ethyl acetate-hexane (1:10˜5) as the eluent to afford 10 as white solid (2.89 g; 62% yield): 1H NMR (400 MHz, CDCl3) δ 7.42-7.48 (m, 6H, six of ArH), 7.27-7.33 (m, 6H, six of ArH), 7.20-7.27 (m, 3H, three of ArH), 5.26 (s, 1H, one of C═CH2), 5.17 (s, 1H, one of C═CH2), 4.13 (d, J=6.1 Hz, 2H, CH2OH), 3.70 (s, 2H, Ph3COCH2), 1.72 (t, J=6.1 Hz, 1H, CH2OH); 13C NMR (100 MHz, CDCl3) δ 145.4, 143.6, 128.3, 127.6, 126.8, 111.6, 87.0, 65.3, 64.5, (8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796432B2
Source datasetuspto-grants-2014_08
ORD IDord-ad7be7d4da6643169981220da4903ded
Source noteuspto-grants-2014_08