HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885756Generated: October 31, 2026
Formaldehyde → 2-Ethyl 2-(hydroxymethyl)hexanal
https://huagongshe.com/reaction/1885756
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Ethylhexanal | HCID 31241 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Ethyl 2-(hydroxymethyl)hexanal | HCID 12538467 | — |
Reaction Steps
A one liter Parr autoclave was charged with 2-ethylhexanal (334 g, 406 mL, 2.6 mole), 44% aqueous formaldehyde (136.4 g, 122 mL, 2.0 mole) and varying amounts of triethylamine to determine the effect of increasing triethylamine concentration on reaction rate. After purging with nitrogen, the autoclave was sealed and heated at 100° C. for one hour. The autoclave was cooled and the contents were analyzed for formaldehyde (HCHO) by calorimetric analysis and for 2-ethyl2-(hydroxymethyl)hexanal (EHMH) by gas chromatography analysis. The yield of EHMH was calculated based on the 2-ethylhexanal consumed which was determined after correcting the gas chromatograph area for methanol and excess 2-ethylhexanal. Table I sets forth the amount of triethylamine (TEA, g/mL), the concentration by weight of triethylamine based on the total weight of the materials charged (TEA, %), the mole percent of formaldehyde converted (HCHO Conv.) and the percent yield of EHMH obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05146004 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-74f401a3cb56486fbafbcfcfc7cd982f |
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| Source note | uspto-grants-1992_09 |
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