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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046444Generated: October 30, 2026

Hydrochloric Acid → 2,2-Dimethyl-3-(tetrahydro-furan-3-yloxy)-propan-1-ol

https://huagongshe.com/reaction/1046444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantDimethyl-3-(tetrahydro-furan-3-yloxy)-propionic acid methyl esterHCID 58114071—
SolventDichloromethaneHCID 6344—
Product2,2-Dimethyl-3-(tetrahydro-furan-3-yloxy)-propan-1-olHCID 6685014882.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

DIBAL (1.74 mL of a 1.0 M solution in hexanes) was added dropwise to a solution of 2,2-dimethyl-3-(tetrahydro-furan-3-yloxy)-propionic acid methyl ester (353 mg, 1.74 mmol) in dichloromethane (9.0 mL) at −78° C. After 2 h at this temperature, an additional equivalent of DIBAL was added and after 1 h the reaction was warmed to 0° C. After an additional 1 h at 0° C., 1.0 N HCl was added dropwise to quench the reaction. The reaction was warmed to room temperature and partitioned between dichloromethane and brine. The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were dried over Na2SO4 and concentrated to give an oil. Purification by flash column chromatography on silica gel using 50% ethyl acetate in hexanes provided 2,2-dimethyl-3-(tetrahydro-furan-3-yloxy)-propan-1-ol (250 mg, 82%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569302B2
Source datasetuspto-grants-2013_10
ORD IDord-495bdd5baf224f5aaa9e09bc3566cdd4
Source noteuspto-grants-2013_10