HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922497Generated: October 30, 2026
Phenyl chloroformate → HCID 57343393, compound
https://huagongshe.com/reaction/1922497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | HCID 53392264 | HCID 53392264 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57343393 | HCID 57343393 | 72.7% |
Reaction Steps
To a stirred solution of N,N-dimethyl-3-(6-nitro-3,4-dihydroquinolin-1(2H)-yl)propan-1-amine (1 g, 3.80 mmol) in dichloromethane (20 ml) was added phenyl carbonochloridate (0.715 ml, 5.70 mmol). The resulting solution was stirred at room temperature overnight. The reaction mixture was then diluted with water and extracted with dichloromethane (3×). The combined organics were dried, filtered and concentrated, then chromatographed in 50-100% ethyl acetate in hexanes, giving the desired phenyl methyl(3-(6-nitro-3,4-dihydroquinolin-1(2H)-yl)propyl)carbamate (1.02 g, 2.76 mmol, 72.7% yield). 1H NMR (DMSO-d6) δ 7.88 (t, J=7 Hz, 1H), 7.78 (s, 1H), 7.37 (t, J=7 Hz, 2H), 7.20 (t, J=7 Hz, 1H), 7.12-7.06 (m, 2H), 6.70 (d, J=9 Hz, 1H), 3.50-3.33 (m, 6H), 3.06, 2.93 (2s, 3H), 2.76-2.71 (m, 2H), 1.92-1.81 (m, 4H). ESI-MS (m/z, %) 370 (MH+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08173813B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-16db1db89d394c67815a45e7e16a440e |
|---|
| Source note | uspto-grants-2012_05 |
|---|