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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483160Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 117857475, compound

https://huagongshe.com/reaction/1483160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantCyclobutanecarbaldehydeHCID 12431621—
ReactantHCID 117857646HCID 117857646—
SolventDichloromethaneHCID 6344—
ProductHCID 117857475HCID 117857475102.8%

Reaction Steps

To a solution of cyclobutane carboxaldehyde (19.45 g, 231.2 mmol) in dichloromethane (500 mL) was added (4R,4aR,7aR,12bS)-1,2,3,4,4a,5,6,7a-octahydrospiro[4,12-methanobenzofuro[3,2-e]isoquinoline-7,2′-[1,3]dioxolane]-9-carbonitrile (25 g, 77.1 mmol). The reaction was stirred for 60 minutes at room temperature before sodium triacetoxyborohydride (32.7 g, 154.0 mmol) was added portionwise over 20 minutes. After one hour, the reaction was quenched with NaHCO3 solution and extracted with dichloromethane (×3). The dichloromethane phases were combined, washed with brine, dried over MgSO4 and concentrated under reduced pressure. The residue was purified by silica chromatography eluted with dichloromethane to 7% methanol in dichloromethane to give (4R,4aR,7aR,12bS)-3-(cyclobutylmethyl)-1,2,3,4,4a,5,6,7a-octahydrospiro[4,12-methanobenzofuro[3,2-e]isoquinoline-7,2′-[1,3]dioxolane]-9-carbonitrile (31.1 g, 98% pure LCMS, assume quant.); [M+H]+ 393.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416137B2
Source datasetuspto-grants-2016_08
ORD IDord-0646144344b74ff19218eaed9a95205d
Source noteuspto-grants-2016_08