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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903517Generated: October 30, 2026

Hydrochloric Acid → HCID 20216757, compound

https://huagongshe.com/reaction/1903517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant13-methyltetradecanalHCID 11085507—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20216757HCID 2021675752.6%

Reaction Steps

Activated zinc (118 mg), a small crystal of iodine, and tetrahydrofuran (3 ml) were stirred and heated under reflux. To the mixture was added a solution of tert-butyl bromoacetate (312 mg) and 13-methyltetradecanal (226 mg) in tetrahydrofuran (3 ml), and the reactants were stirred and heated under reflux for 1 hour. Anhydrous conditions were maintained throughout the experiment. The cooled solution was poured into 0.1 N hydrochloric acid (5.6 ml) and the pH was adjusted to 2.0 with 2 N hydrochloric acid. The excess of zinc was filtered off and the crude products were extracted with ethyl acetate. The ethyl acetate solution was washed with aqueous sodium hydrogen carbonate and brine, and then dried over magnesium sulfate. The ethyl acetate was evaporated off under reduced pressure to give the crude ester, which was purified by column chromatography on silica gel (Merck) and eluted with a mixture of cyclohexane and ethyl acetate (19:1). The fractions containing the object compound were combined and concentrated under reduced pressure. The residue was dried by high vacuum pump to afford an oil of tert-butyl 3-hydroxy-15-methylhexadecanoate (180 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436726
Source datasetuspto-grants-1984_03
ORD IDord-8c4c9ad1ab0b4e27bbfc9a789c82cbec
Source noteuspto-grants-1984_03