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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916279Generated: October 31, 2026

Formaldehyde → HCID 23124995, compound

https://huagongshe.com/reaction/916279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDiisopropylamineHCID 7912—
ReactantMethyl 2-ethylhexanoateHCID 102491—
ReactantButyllithiumHCID 178418339—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 23124995HCID 23124995—

Reaction Conditions

Temperature-20 °C

Reaction Steps

9.8 ml (0.070 mol) of diisopropylamine are added dropwise at 20° C. to a solution of 24.4 ml (0.065 mol) of n-butyllithium (2.7 M in heptane) in 25 ml of MTBE, and the mixture is stirred at −20° C. for 30 min. Within approx. 10 min, 10 g (0.063 mol) of methyl 2-ethylhexanoate are added dropwise at −20° C., and the mixture is stirred at 20° C. for a further 30 min and subsequently admixed with 5.7 g (0.19 mol) of paraformaldehyde. After 30 min at −20° C., the mixture is stirred at 0° C. for 2 h. After the removal of the solvent at 20° C. and 20 mbar, 20 ml of MTBE and 40 ml of saturated aqueous solution of ammonium chloride are added to the oily residue (approx. 20 g) and the mixture is stirred at RT for 2 h. The organic phase is removed, the aqueous phase is re-extracted 1× with 20 ml of MTBE and the combined organic phases are concentrated on a rotary evaporator. The yield of pure product is 86% (GC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268253B2
Source datasetuspto-grants-2007_09
ORD IDord-b4468eaf9b444a31ac70fa7b921d9879
Source noteuspto-grants-2007_09