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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34409Generated: October 26, 2026

Potassium Carbonate → 1-[2-(Tetrahydropyran-2-yloxy)ethyl]-4-(3-hydroxypropy)benzene

https://huagongshe.com/reaction/34409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-1-propanolHCID 12308—
Reactant4-(2-Tetrahydropyran-2-yloxyethyl)phenolHCID 14208783—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-[2-(Tetrahydropyran-2-yloxy)ethyl]-4-(3-hydroxypropy)benzeneHCID 7042019973.6%

Reaction Steps

To a solution of 4-(2-tetrahydropyran-2-yloxyethyl)phenol (9, 8.0 g, 36 mmoles) in 2-butanone (100 mL) were added K2CO3 (10.0 g, 72 mmoles) and 3-bromopropanol (6.5 mL, 72 mmoles). The solution was refluxed 18 hours with mechanical stirring. After cooling, the mixture was filtered and the solvent removed under reduced pressure to afford 13.0 g of crude oil. This was purified by flash chromatography on silica gel (solvent=80:20 ethyl acetate:heptane). The pure fractions were pooled and the solvent removed in vacuo to give 7.0 g of 1-[2-(tetrahydropyran-2-yloxy)ethyl]-4-(3-hydroxypropy)benzene (10). NMR (CDCl3)δppm: 7.0(q, 4H); 4.58(s, 1H)' 4.3-3.3(m, 8H); 3.06(s, 1H); 2.83(t, 2H); 1.83(m, 2H); 1.63(m, 6H). (Scheme II, Step 5.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761420
Source datasetuspto-grants-1988_08
ORD IDord-0d3e6905d57546e0bc7c52aceb0a152e
Source noteuspto-grants-1988_08