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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417621Generated: October 26, 2026

Acetic Acid → 1-(3,4,5-Trimethoxyphenyl)-2-nitro-1,3-propanediol

https://huagongshe.com/reaction/2417621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChloroformHCID 6212—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantNitroethanolHCID 22056827—
SolventMethanolHCID 887—
SolventN-MethylpiperidineHCID 12291—
Product1-(3,4,5-Trimethoxyphenyl)-2-nitro-1,3-propanediolHCID 13468887—

Reaction Steps

19.6 g (0.1 moles) of 3,4,5-trimethoxybenzaldehyde and 9.1 g (0.1 moles) of nitroethanol are suspended in a mixture of 25 ml of methanol and 1 ml of N-methylpiperidine at a temperature of 0° C. (under cooling with ice water). The reaction mixture is stirred for 6 hours, then 50 ml of chloroform are added, the mixture is allowed to stand at 0° C. for 72 hours and then acidified with 1 ml of acetic acid. The separated crystalline substance is filtered off, washed with chloroform and ice-cold (0° C.) water and dried. 19.7 g 68.64%) of 1-(3,4,5-trimethoxyphenyl)-2-nitro-1,3-propanediol are obtained; m.p.: 155°-159° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469703
Source datasetuspto-grants-1984_09
ORD IDord-5802cf88c82f4a039286fd237ccba50f
Source noteuspto-grants-1984_09