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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842048Generated: November 2, 2026

o-Fluorobenzaldehyde → HCID 56941067, compound

https://huagongshe.com/reaction/1842048

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSodiumHCID 5360545—
ReactantHCID 56941370HCID 56941370—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 56941067HCID 56941067—

Reaction Steps

In a flask, dichloromethane (0.5 mL) and acetic acid (3drops) was added to N-(3-(pyridin-4-yl)-1H-indazol-5-yl)morpholine-2-carboxamide (0.014 g, 0.0443 mmol) and 2-fluorobenzaldehyde (0.0112 g, 0.09 mmol). The reaction was stirred for 15 minutes. Sodium triacetoxyborohydride (0.040 g, 0.177 mmol) was added in one portion. The reaction was stirred for an additional 16 hours. Saturated sodium bicarbarbonate (1 mL) was added. The reaction was stirred for an additional 5 minutes and was extracted with dichloromethane (3×1 mL). The extracts were combined, dried with anhydrous sodium sulfate, filtered, and concentrated in vacuo. The resulting crude product was purified by prep LC/MS. LC-MS: 432.2 [M+H]. LC/MS RT0.869 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946216B2
Source datasetuspto-grants-2015_02
ORD IDord-2273f8b794d9485caba75590d46699bb
Source noteuspto-grants-2015_02