HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606265Generated: October 29, 2026
1,2-Dichloroethane → (1,3-Dihydroisobenzofuran-1-yl)-(piperidin-4-yl)methanone hydrochloride
https://huagongshe.com/reaction/606265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | (1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanone | HCID 22248144 | — |
| Solvent | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Product | (1,3-Dihydroisobenzofuran-1-yl)-(piperidin-4-yl)methanone hydrochloride | HCID 22248211 | — |
Reaction Steps
After dissolving 517 mg of (1-benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanone in 5 ml of 1,2-dichloroethane, 0.49 ml of 1-chloroethyl chloroformate was added and the mixture was heated to reflux for 1 hour. The reaction solution was distilled off under reduced pressure, 5 ml of methanol was added to the residue and heating to reflux was continued for 1 hour. The reaction solution was distilled off under reduced pressure, saturated aqueous sodium bicarbonate solution was added and extraction was performed with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure to obtain 104 mg of (1,3-dihydroisobenzofuran-1-yl)-(piperidin-4-yl)methanone hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07915274B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-c88eded4398446a2a0e07f62362c7741 |
|---|
| Source note | uspto-grants-2011_03 |
|---|