HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372908Generated: October 30, 2026
Sodium Chloride → 7-benzyloxy-5-oxiranyl-1H-quinolin-2-one
https://huagongshe.com/reaction/1372908
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 7-(Benzyloxy)-5-(chloroacetyl)quinolin-2(1H)-one | HCID 21072859 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-benzyloxy-5-oxiranyl-1H-quinolin-2-one | HCID 57469371 | — |
Reaction Steps
Lithium borohydride (434 mg, 19.93 mmol) is added to a suspension of 7-benzyloxy-5-(2-chloroacetyl)-1H-quinolin-2-one (6 g, 18.31 mmol) in THF (150 mL) at 0–5 ° C. and the mixture is stirred for 30 minutes. 2.5 N sodium hydroxide solution (43 mL, 107.50 mmol) is added and the mixture is stirred for 2 hours at 5–10 ° C. and for 2.5 hours at ambient temperature. Then the reaction mixture is slowly combined with glacial acetic acid (6.5 mL) followed by semi-saturated sodium chloride solution (100 mL) and stirred for a further 5 minutes. The precipitate formed is filtered off and the aqueous phase is extracted with ethyl acetate/THF (1/1.5×100 mL). The solid filtered off and the organic phases are combined, dried with sodium sulphate and evaporated down. The crude product is stirred with methanol (30 mL) and the precipitate is filtered off and dried at ambient temperature. Yield: 4.8 g (89%); mass spectroscopy: [M+H]+=294.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160882B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-6845c1ac79874eb4baf5c123ff4797e7 |
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| Source note | uspto-grants-2007_01 |
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