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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505013Generated: November 1, 2026

Formaldehyde → 2-Nitro-2-(4-octylphenethyl)propane-1,3-diol

https://huagongshe.com/reaction/1505013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant1-(3-Nitropropyl)-4-octylbenzeneHCID 11150103—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Nitro-2-(4-octylphenethyl)propane-1,3-diolHCID 66837276—

Reaction Conditions

Temperature27.5 °C

Reaction Steps

1-(3-Nitropropyl)-4-octylbenzene (37 g) and methanol (190 mL) are charged into a round bottom flask and stirred at 25-30° C. Paraformaldehyde (37 g) and triethylamine (38.52 g) are charged into the flask and the reaction mixture is heated to a reflux temperature (about 68° C.). The reaction mixture is maintained at the same temperature for about 2 hours and is cooled to a temperature of 25-30° C. The reaction mixture is evaporated under reduced pressure at a temperature of about 45° C. to obtain crude compound. Water (190 mL) and ethyl acetate (190 mL) are charged to the crude compound, stirred, and the organic layer is separated. The aqueous layer is extracted with ethyl acetate (190 mL) and the organic layer is combined with the initial organic layer. The combined organic layer is washed with water (190 mL) followed by brine solution (190 mL), dried over sodium sulphate, and evaporated under reduced pressure. Hexane (370 mL) is charged at 28° C. and the reaction mass is stirred at the same temperature for about 1 hour. The solid obtained is collected by filtration, washed with hexane (37 mL), and dried at 28° C. for about 3 hours to give 20.5 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216943B2
Source datasetuspto-grants-2015_12
ORD IDord-bb46b7aed1194b2db0a25275655e3083
Source noteuspto-grants-2015_12