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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503078Generated: October 31, 2026

Hydrochloric Acid → HCID 69098014, compound

https://huagongshe.com/reaction/1503078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-MethyltetrahydrofuranHCID 7301—
Reactant144728-22-3HCID 54153109—
ReactantHCID 178418573HCID 178418573—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 69098014HCID 69098014—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 4.4 g 6-oxa-spiro[2.5]octane-5,7-dione (31 mmole) in 66 ml tetrahydrofuran are added 600 mg copper(I)chloride (6 mmole, 0.2 eq). The mixture is cooled to −20° C. and 9.8 ml of methylmagnesium bromide in 2-methyl tetrahydrofuran (3.2 M solution in 2-methyl tetrahydrofuran, 31 mmole, 1.0 eq) are added dropwise over 0.5 hours. The mixture is warmed to room temperature and stirred for 2 hours. 66 ml of water are added and the mixture is acidified to pH 3.0 by addition of 20.4 g of 2 M hydrochloric acid. 50 ml of methyl tert-butyl ether are added and the phases are separated. The aqueous phase is extracted again with 50 ml of methyl tert-butyl ether and the combined organic phases are washed with 20 ml of brine and concentrated to dryness. The resulting crude product is directly used in the next step (esterification to [1-(2-oxo-propyl)-cyclopropyl]-acetic acid methyl ester).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212120B2
Source datasetuspto-grants-2015_12
ORD IDord-a0347d69968a45ba977e482e3d6ea224
Source noteuspto-grants-2015_12