Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396669Generated: November 2, 2026

Sodium Bicarbonate → HCID 86701158, compound

https://huagongshe.com/reaction/1396669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantDimethylamine tetrahydrofuranHCID 22320367—
Reactant1,1-Dimethylethyl 4-formyl-1,3-dihydro-2H-isoindole-2-carboxylateHCID 50999120—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductHCID 86701158HCID 86701158—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 238 mg of tert-butyl 4-formyl-1,3-dihydro-2H-isoindole-2-carboxylate, 612 mg of sodium triacetoxyborohydride, 963 μL of a 2 M dimethylamine-tetrahydrofuran solution, 12 μL of acetic acid, and 14 mL of 1,2-dichloroethane was stirred at 60° C. overnight. After cooling to room temperature, to the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and chloroform was added and the aqueous layer was separated. The obtained organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 123 mg of tert-butyl 4-[(dimethylamino)methyl]-1,3-dihydro-2H-isoindole-2-carboxylate as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901126B2
Source datasetuspto-grants-2014_12
ORD IDord-61c37b59b1ee44c2953c90ee6aade00d
Source noteuspto-grants-2014_12