HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47147Generated: October 29, 2026
Methyl chloroformate → (R)-methyl 1-methoxy-2-oxo-1,2,3,4-tetrahydroquinolin-3-ylcarbamate
https://huagongshe.com/reaction/47147
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 54379478 | HCID 54379478 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | (R)-methyl 1-methoxy-2-oxo-1,2,3,4-tetrahydroquinolin-3-ylcarbamate | HCID 10538623 | 99% |
Reaction Steps
A solution of methyl chloroformate (42.8 g, 0.453 mol) in chloroform (50 ml) was added to a mixture of (R)-1,2,3,4-tetrahydro-1-methoxy-2-oxo-3-quinolinamine 1 (M. Kawase, T. Kitamura, Y. Kikugawa, J. Org. Chem., 54, 1989 3394-3403)(0.15 mol) and sodium bicarbonate (50.4 g, 0.600 mol) in chloroform (250 ml) and water (100 ml) over a period of 10 minutes at 0° C. The mixture was stirred overnight at room temperature, diluted with pentane, and the layers were separated. The aqueous layer was extracted with diethylether, and the combined organic extracts were washed with brine and dried (MgSO4). The solvent was removed under vacuum to leave an amber oil. Purification by flash chromatography (230-400 mesh silica gel, 35-40% ethyl acetate in hexane) gave the title compound as a light yellow oil (37.0 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE038452E1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-be29fffb480243e1ab7503e32357e27d |
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| Source note | uspto-grants-2004_03 |
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