HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916283Generated: October 30, 2026
Hydrochloric Acid → 2-ethyl-2-(hydroxymethyl)hexanoic Acid
https://huagongshe.com/reaction/916283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Ethylhexanoic Acid | HCID 8697 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-ethyl-2-(hydroxymethyl)hexanoic Acid | HCID 9793987 | — |
Reaction Steps
113 ml (0.305 mol) of n-butyllithium (2.7 M in heptane) are added dropwise at 0° C. to a solution of 46 ml of disiopropylamine (0.327 mol) in 320 ml of THF and the mixture is stirred at 0° C. for 30 min (Solution 1). 40 g (0.277 mol) of 2-ethylhexanoic acid are added dropwise at 25° to a suspension of 7 g of NaH 95% (0.277 mol) in 320 ml of THF within approx. 15 min, and the reaction mixture is stirred at 50° C. for 30 min (Solution 2). Solution 1 is added at 0° C. to Solution 2 and subsequently heated to 50° C. for 1.5 h. The clear solution is cooled to 0° C. and admixed with 25 g (0.833 mol) of paraformaldehyde. After 10 min, the mixture is stirred at RT for 18 h. The mixture is admixed with saturated aqueous solution of ammonium chloride and adjusted to pH=1-2 with 6N HCl. The organic phase is removed, the aqueous phase is re-extracted 1× with MTBE and the combined organic phases are concentrated on a rotary evaporator. The yield of pure product is 71% (GC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268253B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-e08e2db190e14f048db110a230d6686d |
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| Source note | uspto-grants-2007_09 |
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