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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039428Generated: October 26, 2026

2-Nitropropane → 6-Methyl-3,7-dinitrononan-4-ol

https://huagongshe.com/reaction/1039428

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitropropaneHCID 398—
Reactant1-NitropropaneHCID 7903—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCrotonaldehydeHCID 447466—
Product6-Methyl-3,7-dinitrononan-4-olHCID 58308990—

Reaction Steps

A three neck round bottom flask equipped with a stir bar, thermocouple, dropping funnel capped with nitrogen inlet and condenser was charged with 2-Nitropropane (50 g, 0.56 mols, 5.0 equivalents) and catalytic amount of DBU. The deep yellow solution was mixed under nitrogen for about thirty minutes. To this mixture was added crotonaldehyde (7.9 g, 9.2 mL, 0.112 moles, 1.0 equivalent) drop-wise over a period of twenty minutes. The addition of crotonaldehyde in this case was done at room temperature and during addition, exotherm of about 12° C.-15° C. was observed. After complete addition, the reaction was stirred at room temperature for 6 hours. At this point, GC analysis showed the absence of crotonaldehyde from the mixture. The reaction was let to stir at room temperature overnight and high performance liquid chromatography (HPLC) analysis showed the presence of only two peaks which correspond to 1-NP which was in excess and the desired product (1 CA+2NP adduct). Excess 1-NP was removed by vacuum distillation and the resulting orange viscous liquid was subjected to hydrogenation. This material was about 37.2 g total weight however it still had some 1-NP remaining.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552072B2
Source datasetuspto-grants-2013_10
ORD IDord-5a9907e3e7c347f8a38ada903d21423e
Source noteuspto-grants-2013_10