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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78291Generated: October 25, 2026

Acetic Acid → 5-(2-Nitro-ethyl)-2-phenoxy-pyridine

https://huagongshe.com/reaction/78291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantVertellusHCID 22959485—
Reactant5-((E)-2-Nitro-vinyl)-2-phenoxy-pyridineHCID 59255295—
SolventDimethyl SulfoxideHCID 679—
Product5-(2-Nitro-ethyl)-2-phenoxy-pyridineHCID 57626341—

Reaction Steps

To a solution of 5-((E)-2-nitro-vinyl)-2-phenoxy-pyridine described in Manufacturing Example 232-1-3 (5.97 g, 24.6 mmol) and acetic acid (3.2 mL) in dimethyl sulfoxide (52 mL) was added sodium borohydrate (1.4 g, 36.9 mmol), at room temperature while cooling appropriately. This mixture was stirred for 30 minutes at room temperature. This mixture was cooled appropriately, then, water was added, which was stirred for 30 minutes at room temperature. This mixture was liquid-separated, and the organic layer was separated. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (5.72 g) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-efc1858a1c6441eb9518561be2d4d2e2
Source noteuspto-grants-2014_09