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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294494Generated: November 1, 2026

Sodium borohydride → HCID 23433598, compound

https://huagongshe.com/reaction/2294494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23433650HCID 23433650—
ProductHCID 23433598HCID 2343359884%

Reaction Conditions

Temperature0 °C

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 methylanol (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 1-tert-butyloxycarbonyl-1,2,3,4-tetrahydro-3,3-dimethylquinoline:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688810
Source datasetuspto-grants-1997_11
ORD IDord-5a30f7880bfa47de923ec4f251eec862
Source noteuspto-grants-1997_11