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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367720Generated: October 26, 2026

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

https://huagongshe.com/reaction/2367720

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 mots, 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 (1CA+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 numberUS08697915B2
Source datasetuspto-grants-2014_04
ORD IDord-53d4cc08095a41ecad4ed51466e9b2e5
Source noteuspto-grants-2014_04