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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213039Generated: October 29, 2026

Sodium borohydride → HCID 69559203, compound

https://huagongshe.com/reaction/2213039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 53446371HCID 53446371—
ProductHCID 69559203HCID 6955920399%

Reaction Steps

A solution of 1-(1,1-dimethylethyl) 4-phenylmethyl 4-(3-butenyl)-1,4-piperidinedicarboxylate (Description 135, 1.06 g, 2.84 mmol) in dichloromethane/methanol (50:50, 20 mL) was cooled to −78° C. and oxygen was bubbled through the mixture for 10 minutes. Ozone was bubbled through the mixture until a blue coloration persisted. Oxygen was bubbled through the mixture for 10 minutes, then nitrogen for 10 minutes. Sodium borohydride (1.1 g, 28.9 mmol) was added over 5 minutes and the mixture was allowed to warm to room temperature. The solvent was evaporated under reduced pressure and water (40 mL) was added. The mixture was extracted with ethyl acetate (3×40 mL), the combined organic fractions were dried (Na2SO4) and the solvent was evaporated under reduced pressure to give the title compound (1.06 g, 99%). 1H NMR (400 MHz, CDCl3) δ 7.4–7.3 (5H, m), 5.15 (2H, s), 3.95–3.75 (2H, m), 3.52 (2H, t, J 7 Hz), 2.95–2.80 (2H, m), 2.12 (2H, br d, J 10 Hz), 1.65–1.30 (7H, m), and 1.44 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105507B2
Source datasetuspto-grants-2006_09
ORD IDord-17c494f2d8194592ab1c955d91a088bc
Source noteuspto-grants-2006_09