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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870919Generated: October 30, 2026

Sodium borohydride → HCID 86695915, compound

https://huagongshe.com/reaction/870919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86695912HCID 86695912—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86695915HCID 8669591599.5%

Reaction Steps

To a stirred solution of 2-amino-4-(4-chloro-2-fluorophenyl)nicotinaldehyde (50 mg, 0.199 mmol) in MeOH (2 mL) and THF (5 mL) was added sodium borohydride (9.06 mg, 0.239 mmol) then the solution was stirred for 1 h. The volatile organics were removed under reduced pressure and the residue was quenched by addition of saturated aqueous ammonium chloride solution (10 mL). The reaction mixture was extracted with CH2Cl2 (2×10 mL). The combined organic extracts were washed with brine (1×10 mL), dried over sodium sulfate and concentrated under reduced pressure to yield (2-amino-4-(4-chloro-2-fluorophenyl)pyridin-3-yl)methanol (50 mg, 0.198 mmol, 21% yield for two steps). LCMS (ESI) m/e 253 [(M+H)+, calcd for C12H11ClFN2O 253.0]; LC/MS retention time (Method C): tR=1.48 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969564B2
Source datasetuspto-grants-2015_03
ORD IDord-3604248b86ab4a6ba92e621bb1797868
Source noteuspto-grants-2015_03