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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099829Generated: October 25, 2026

Dichloromethane → 4-Tert-Butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinate

https://huagongshe.com/reaction/2099829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron trifluoride etherateHCID 8000—
ReactantTert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
Reactant4-methoxy-3-((7-methyl-1H-indazol-5-yl)methyl)-4-oxobutanoic acidHCID 18452115—
SolventTetrahydrofuranHCID 8028—
Product4-Tert-Butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinateHCID 57794720—

Reaction Steps

To a solution of 4-methoxy-3-((7-methyl-1H-indazol-5-yl)methyl)-4-oxobutanoic acid (0.9764 g, 3.54 mmol) and t-butyl-2,2,2-trichloroacetoimidate (3.78 mL, 21.22 mmol) in tetrahydrofuran (25 mL) was added 1M boron trifluoride etherate (0.2 mL) at room temperature. Heat generation was observed and the reaction was stirred for 3.5 h before passing it through a pad of silica gel. Evaporation of the filtrate gave a white solid. Methylene chloride (20 mL) was added and the resulting white solid was removed by filtration. The filtrate was concentrated and the final product was obtained via silica gel chromatography eluting with 0% to 50% ethyl acetate/hexane. (0.605 g, 52%) HPLC tR=1.51 min, MS(ESI)[M+H]+=332.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569578B2
Source datasetuspto-grants-2009_08
ORD IDord-aa6066628f6c40c8b75a75fca9f74d27
Source noteuspto-grants-2009_08