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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908181Generated: October 28, 2026

Lithium borohydride → HCID 58551033, compound

https://huagongshe.com/reaction/1908181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 58551224HCID 58551224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58551033HCID 5855103366.1%

Reaction Steps

2-Isopropoxy-5-(1-methylspiro[chromeno[4,3-c]pyrazole-4,4′-piperidine]-1′-carbonyl)benzaldehyde (110 mg, 0.25 mmol) was dissolved in THF (3 mL) and LiBH4 (11 mg, 0.50 mmol) was added. The reaction was stirred at room temperature for 1.5 h before being quenched with methanol (3 mL). The reaction was neutralized by the addition of a saturated sodium bicarbonate solution and was extracted with ethyl acetate (3×). The combined organic layers were dried over Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel (0-100% ethyl acetate in hexane) to yield [3-(hydroxymethyl)-4-isopropoxy-phenyl]-(1-methylspiro[chromeno[4,3-c]pyrazole-4,4′-piperidine]-1′-yl)methanone (74 mg, 65%) as a white solid. ESI-MS m/z calc. 447.5. found 448.3 (M+1)+. Retention time: 1.59 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-bb32d5c521684bed8608559ca4781b2a
Source noteuspto-grants-2013_12