HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396669Generated: November 2, 2026
Sodium Bicarbonate → HCID 86701158, compound
https://huagongshe.com/reaction/1396669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| Reactant | 1,1-Dimethylethyl 4-formyl-1,3-dihydro-2H-isoindole-2-carboxylate | HCID 50999120 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86701158 | HCID 86701158 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08901126B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-61c37b59b1ee44c2953c90ee6aade00d |
|---|
| Source note | uspto-grants-2014_12 |
|---|