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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939330Generated: October 25, 2026

Hydrochloric Acid → 3-Methoxypentane-1,5-diol

https://huagongshe.com/reaction/1939330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl triflateHCID 9526—
Reactant2,6-Di-tert-butylpyridineHCID 68510—
ReactantDiethyl 3-hydroxyglutarateHCID 96259—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxypentane-1,5-diolHCID 22101218—

Reaction Conditions

Temperature-5 °C

Reaction Steps

25 ml of methyl trifluoromethylsulfonate are added to a solution of 30 g of diethyl 3-hydroxyglutarate and 33 ml of 2,6-di-tert-butylpyridine in 500 ml of DCM and the mixture is refluxed for 5 hours. After cooling, 500 ml of a 0.5N solution of HCl are added, the organic phase is decanted and dried over magnesium sulfate and the solvent is evaporated off under vacuum. The solid obtained is taken up with 200 ml of anhydrous THF, the mixture is filtered and the filtrate is then cooled to -5° C. 160 ml of a 1M solution of lithium aluminum hydride in THF are then added slowly and the mixture is stirred for 16 hours, the temperature being allowed to rise to RT. The reaction mixture is cooled to 0° C. and 5.5 ml of water, 18 ml of a 15% solution of NaOH and 5.5 ml of water are added successively. The mineral salts are filtered off and the filtrate is evaporated under vacuum to give the expected product after distillation under reduced pressure. B.p.=104° C. under 1.5 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696145
Source datasetuspto-grants-1997_12
ORD IDord-c06d5392d64949fb9b7e8e9fac97b104
Source noteuspto-grants-1997_12