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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427414Generated: November 1, 2026

Sodium borohydride → HCID 68001651, compound

https://huagongshe.com/reaction/1427414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86687800HCID 86687800—
SolventMethanolHCID 887—
ProductHCID 68001651HCID 6800165169%

Reaction Steps

To a suspension of the aldehyde obtained above (850 mg, 5.1 mmol) in MeOH (25 mL) at 0° C. was added sodium tetrahydroborate (190 mg, 5.10 mmol) and the reaction mixture warmed to RT for 2 hr and then quenched by the addition of hydrochloric acid (1 M, 5.0 mL) The mixture was diluted with sat aq. NaHCO3 (40 mL) and was extracted with DCM (80 mL, 6×100 mL). The combined organic extracts were dried and evaporated in vacuo to afford (2-amino-3-nitropyridin-4-yl)methanol as an orange solid (630 mg, 69%); Rt 0.40 min (Method 2); m/z 170 (M+H)+, (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933228B2
Source datasetuspto-grants-2015_01
ORD IDord-1cfc0b70379a4fbeb6329d131a861329
Source noteuspto-grants-2015_01