HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604816Generated: November 1, 2026
Sodium borohydride → HCID 23433598, compound
https://huagongshe.com/reaction/1604816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23433650 | HCID 23433650 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23433598 | HCID 23433598 | 84% |
Reaction Steps
To a solution of 1-tert-butyloxycarbonyl-1,2,3,4-tetrahydro-3,3-dimethyl-4- quinolinone (128 mg, 0.47 mmol) in methanol (2 mL) at 0° C. was added portionwise sodium borohydride (18 mg, 0.47 mmol) and the reaction mixture was stirred at 0° C. for 3 h. The reaction mixture was then quenched with sat'd NH4Cl (2 mL), extracted with ethyl acetate (2×5 mL), dried (Na2SO4) and concentrated A solution of this crude material in ethyl acetate (3 mL) was hydrogenated under an atmosphere of hydrogen with 10% Pd/C (20 mg) and a trace of conc. H2SO4 at rt for 16 h. Filtration over Celite™ afforded 100 mg (84%) of 1-tert-butyloxycarbonyl-1,2,3,4-tetrahydro-3,3-dimethylquinoline. Data for
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994544 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-4dddb303b4b14aa58219bc8e89d4ac1a |
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| Source note | uspto-grants-1999_11 |
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