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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499113Generated: October 28, 2026

Sodium borohydride → HCID 114845940, compound

https://huagongshe.com/reaction/1499113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 114844633HCID 114844633—
SolventMethanolHCID 887—
ProductHCID 114845940HCID 114845940—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Chloro-2-(3-methyl-pyrazol-1-yl)-benzaldehyde (446 mg, 2.03 mmol) from Step 1 was dissolved in MeOH (14 mL) and cooled to 0° C. NaBH4 (175 mg, 4.61 mmol)) was added portionwise. The reaction mixture was allowed to warm to RT, and after 90 min was quenched with acetone. The MeOH was removed in vacuo. The residue was partitioned between water and EtOAc and then extracted. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Purification by normal phase silica gel column chromatography (EtOAc/heptane) provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199994B2
Source datasetuspto-grants-2015_12
ORD IDord-67343303a01d414fbf6247e5bcb36706
Source noteuspto-grants-2015_12