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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737676Generated: November 2, 2026

Sodium borohydride → HCID 21912450, compound

https://huagongshe.com/reaction/1737676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21912363HCID 21912363—
SolventMethanolHCID 887—
ProductHCID 21912450HCID 2191245049.7%

Reaction Steps

A mixture of 4-[4-(1-ethyl-propoxy)-3,6-dimethyl-pyridin-2-yloxy]-3,5-dimethyl-benzaldehyde (114 mg, 0.41 mmol) and sodium borohydride (63 mg, 1.6 mmol) in 3 ml of methanol was stirred at room temperature for 2 hours. The reaction mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated to give yellow oil. The oil was purified through silica gel using chloroform as eluent to give 70 mg of the title compound as a colorless oil. 1H NMR (CDCl3) δ7.04 (s, 2H), 6.32 (s,1H), 4.55 (s, 2H), 4.21 (m, 1H), 2.30 (brs, 1H), 2.22 (s, 3H), 2.21 (s, 3H), 2.12 (s, 6H), 1.73 (m, 4H), 0.91 (t, 6H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962479
Source datasetuspto-grants-1999_10
ORD IDord-224025d9904f41f8a5f0246c933ba7c3
Source noteuspto-grants-1999_10