Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887239Generated: October 29, 2026

2-Phenylethanol → Phenethyl tosylate

https://huagongshe.com/reaction/1887239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylethanolHCID 6054—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductPhenethyl tosylateHCID 2052251.2%

Reaction Steps

To a stirred solution of phenethyl alcohol (0.50 mL, 4.17 mmol) in pyridine (4 mL) at 0° C. was added p-toluenesulfonyl chloride (0.80 g, 4.18 mmol). The reaction mixture was stirred for 16 h, and then diluted with ethyl acetate (75 mL). The organic solution was washed with 10% aqueous hydrochloric acid (2×25 mL), saturated aqueous sodium bicarbonate (50 mL) and brine (25 mL), then dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue was purified by column chromatography eluting with 0-20% ethyl acetate in hexane to afford the title compound as a light yellow liquid (0.59 g, 51%): 1H NMR (300 MHz, CDCl3) δ 7.69 (d, J=8.3 Hz, 2H), 7.31-7.20 (m, 5H), 7.11 (dd, J=7.4, 1.7 Hz, 2H), 4.21 (t, J=7.1 Hz, 2H), 2.96 (t, J=7.1 Hz, 2H), 2.43 (s, 3H); MS (ES+) m/z 299.2 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501746B2
Source datasetuspto-grants-2013_08
ORD IDord-1bc73511aca9494aa6bb9d051324f4d1
Source noteuspto-grants-2013_08