HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483160Generated: October 30, 2026
Sodium triacetoxyborohydride → HCID 117857475, compound
https://huagongshe.com/reaction/1483160
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Cyclobutanecarbaldehyde | HCID 12431621 | — |
| Reactant | HCID 117857646 | HCID 117857646 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117857475 | HCID 117857475 | 102.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416137B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-0646144344b74ff19218eaed9a95205d |
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| Source note | uspto-grants-2016_08 |
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