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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325813Generated: October 24, 2026

Hydrochloric Acid → Methyl 2-propyl-6-heptenoate

https://huagongshe.com/en/reaction/325813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
ReactantMethyl valerateHCID 12206—
Reactant1-Pentene, 5-bromo-HCID 70704—
ReactantLithium diisopropylamideHCID 2724682—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventButyllithiumHCID 178418339—
ProductMethyl 2-propyl-6-heptenoateHCID 2046287143.2%

Reaction Steps

To a solution of lithium diisopropyl amide, which was prepared from diisopropylamine (6.6 g) in dry tetrahydrofuran (50 ml) and 15% butyl lithium in hexane solution (38 ml) at -65° to -60° C. in a nitrogen atmosphere, were added dropwise a solution of methyl pentanoate (7 g) in dry tetrahydrofuran (65 ml) followed by a solution of 5-bromo-1-pentene (9 g) in dry tetrahydrofuran (30 ml) at the same temperature. The mixture was stirred for 4 hours at -65° to 0° C. All the operations described above were carried out in a nitrogen atmosphere. Diluted hydrochloric acid (25 ml) and toluene (200 ml) were added at 0° C. to the mixture, which was further stirred. The organic layer was separated, washed with water, dried and concentrated. The resulting oily residue (9 g) was purified by silica gel column chromatography to give colorless oil of methyl 2-propyl-6-heptenoate (4.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443365
Source datasetuspto-grants-1984_04
ORD IDord-03a8983bed7549a7883f36fce2efdad2
Source noteuspto-grants-1984_04