Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417625Generated: October 26, 2026

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

https://huagongshe.com/reaction/2417625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant4-NitrobenzaldehydeHCID 541—
ReactantNitroethanolHCID 22056827—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
Product1-(4-Nitrophenyl)-2-nitro-1,3-propanediolHCID 1346890570.24%

Reaction Conditions

Temperature0 °C

Reaction Steps

7.55 g (0.05 moles) of 4-nitrobenzaldehyde and 4.55 g (0.05 moles) of nitroethanol are suspended in a mixture of 30 ml of methanol and 0.2 ml of triethylamine. The mixture is stirred at 0° C. until dissolution (about 30 minutes) and then allowed to stand at 0° C. for 20 hours. The mixture is acidified (pH 2) with 0.2 ml of acetic acid and 0.2 ml of concentrated hydrochloric acid, and 20 ml of ice-cold water are added. The separated crystals are filtered off, washed with chloroform and dried. 8.5 g (70.24%) of 1-(4-nitrophenyl)-2-nitro-1,3-propanediol are obtained; m.p. 105°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469703
Source datasetuspto-grants-1984_09
ORD IDord-bc6d5460c6434353ba32bf5d9543c3fd
Source noteuspto-grants-1984_09