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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3002Generated: October 26, 2026

Hydrochloric Acid → 1-Chloro-3-propyl-2-hexanone

https://huagongshe.com/reaction/3002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantValproic AcidHCID 3121—
ReactantDiazomethaneHCID 9550—
Reactant1,4-DioxaneHCID 31275—
ReactantOxalyl chlorideHCID 65578—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-Chloro-3-propyl-2-hexanoneHCID 10797377—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 2-propylpentanoic acid (156.6 μl, 1.00 mmol) dissolved in anhydrous dichloromethane (2 mL) was added DMF (3 μL, 4 mole %), and the solution was cooled to 0° C. under a nitrogen atmosphere. To the solution was added oxalyl chloride (94.3 μL, 1.08 mmol) dropwise over a few minutes. The reaction was stirred 18 hours while warming to ambient temperature. The mixture was cooled to 0° C. and excess ~0.3M ethereal diazomethane solution was added. The reaction mixture was stirred 18 hours while warming to ambient temperature. The reaction mixture was washed with 1M aqueous sodium carbonate solution (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was dissolved in ether (2mL) and cooled to 0° C. under a nitrogen atmosphere. Hydrogen chloride as a 4N solution in dioxane (275 μL, 1.10 mmol) was added dropwise over a few minutes. The reaction was stirred 18 hours while warming to ambient temperature. The reaction mixture was concentrated under reduced pressure and the residual oil was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731434
Source datasetuspto-grants-1998_03
ORD IDord-9216403abe2a471cb8b491c2ec69c28c
Source noteuspto-grants-1998_03