HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619119Generated: November 1, 2026
Hydrochloric Acid → HCID 21846057, compound
https://huagongshe.com/reaction/619119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21846034 | HCID 21846034 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21846057 | HCID 21846057 | — |
Reaction Steps
0.22 ml (1.58 mmol) of triethylamine is added to a suspension of 0.365 g (1.51 mmol) of 6-cyano-1-methyl-2-oxo-1,2-dihydro-4-quinolineacetic acid in 10 ce of tetrahydrofuran at -10° C., and 0.16 ml (1.6 mmol) of ethyl choroformate is then added dropwise. After stirring at -10° C. for 45 minutes, the reaction medium is filtered and the solids are rinsed with 3×8 ml of tetrahydrofuran. 0.25 g (6.61 mmol) of sodium borohydride and then 0.94 ml of methanol are added to the filtrate at 5-10° C. After stirring at 5-10° C. for 2 hours, 13 ml of 1 N aqueous hydrochloric acid solution are added. The mixture is extracted with is dichloromethane and then with ethyl acetate. The organic phases are dried over sodium sulphate and then concentrated under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958924 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-37278481e19d43a18a9386f07e046676 |
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| Source note | uspto-grants-1999_09 |
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