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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165673Generated: October 30, 2026

Formaldehyde → 2-Nitro-2-isopropyl-1,3-propanediol

https://huagongshe.com/reaction/1165673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-1-nitropropaneHCID 69367—
Product2-Nitro-2-isopropyl-1,3-propanediolHCID 14388187%

Reaction Steps

To a solution of 2-methyl-1-nitropropane (38.7 g, 0.375 mol, prepared by the procedure of N. Kornblum, B. Tunbe, and H. Ungnade, J. Amer. Chem. Soc., 76, 3209 (1954)) and NEt3 (Eastman, 3.79 g, 0.0375 mol) in CH3OH (50 mL) was added dropwise 37% aqueous formaldehyde solution (Mallinckrodt, 76.2 g, 0.938 mol) at a rate such that the reaction mixture temperature did not exceed 30°. After 72 h, the solution was concentrated under vacuum and the residue was dissolved in H2O (250 mL). The solution was continuously extracted for 1 h with CH2Cl2 (1 L). The CH2Cl2 solution was dried (MgSO4), filtered, and concentrated to give 53.3 g (87%) of 2-isopropyl-2-nitro-1,3-propanediol, as a waxy, white solid, mp 67°-72° C. (lit. mp 87°-88°, B. M. Vanderbilt and H. B. Hass, Ind. Eng. Chem. 32, 34 (1940). In our hands this literature procedure failed to give the desired compound).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04910218
Source datasetuspto-grants-1990_03
ORD IDord-672692f460ef4cdaacd08a5d79c75c01
Source noteuspto-grants-1990_03