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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807044Generated: November 1, 2026

Ethyl isobutyrate → Ethyl tetrahydro-4-hydroxy-alpha,alpha-dimethyl-2H-pyran-4-acetate

https://huagongshe.com/reaction/1807044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isobutyrateHCID 7342—
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl tetrahydro-4-hydroxy-alpha,alpha-dimethyl-2H-pyran-4-acetateHCID 6239921392%

Reaction Conditions

Temperature-50 °C

Reaction Steps

Step A To a hexane solution (Aldrich, 2 M) of LDA (78 mL, 160 mmol) in tetrahydrofuran (100 mL) at −50° C. was added a solution of isobutyric acid ethyl ester (Alfa) (17 mL, 127 mmol) in tetrahydrofuran (20 mL) dropwise. The reaction mixture was stirred −50° C. for 1 h, then a tetrahydrofuran solution (10 mL) of tetrahydro-pyran-4-one (Aldrich) (9.8 g, 98 mmol) was added dropwise. The reaction mixture was warmed up to room temperature and stirred for 18 h. Aqueous saturated NH4Cl was added to quench the reaction. The mixture was extracted with ethyl ether. The organic layer was separated, and the aqueous layer was extracted with ethyl ether. The organic layers were combined, washed with brine, water, dried over MgSO4, and concentrated to give 2-(4-hydroxy-tetrahydro-pyran-4-yl)-2-methyl-propionic acid ethyl ester as a yellow oil (19.5 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-72fe4ac9125b46508f194dc4576dc365
Source noteuspto-grants-2013_01