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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797483Generated: November 2, 2026

Tetrahydrofuran → HCID 22175795, compound

https://huagongshe.com/reaction/1797483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 22175327HCID 22175327—
ReactantHCID 178420675HCID 178420675—
SolventWaterHCID 962—
ProductHCID 22175795HCID 2217579592.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-butoxy-6,7-dichloro-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinealdehyde (0.98 g, 24 mmol) in tetrahydrofuran (20 mmol) was added 3N methylmagnesium bromide tetrahydrofuran solution (1.5 ml, 4.5 mmol) at 0° C. and the obtained mixture was stirred at 0° C. for 1 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to give 4-butoxy-6,7-dichloro-3-(1-hydroxyethyl)-2-methyl-1(2H)-isoquinolinone (0.95 g, 92.2%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-99f7a03fb84b4804b6781a33ebce2105
Source noteuspto-grants-2006_04