HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064522Generated: October 31, 2026
Malic Acid → Bis(2-methylbutyl) 2-hydroxybutanedioate
https://huagongshe.com/reaction/1064522
Participants
| Role | Name | HCID | Charge |
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| Reactant | Malic Acid | HCID 525 | — |
| Reactant | 2-Methyl-1-butanol | HCID 8723 | — |
| Product | Bis(2-methylbutyl) 2-hydroxybutanedioate | HCID 18718393 | — |
Reaction Steps
Di(2-methylbutyl)-DL-malate was prepared using a procedure similar to that in Example 4. To the reaction flask, DL-malic acid (100.56 g), 2-methyl-1-butanol (325 mL) and Amberlyst®15 ion exchange resin (15.1 g) were added. The mixture was placed under nitrogen and heated to reflux. At 108° C., two phases started to collect in the Dean-Stark trap. After 1.5 hr, the reaction temperature was increased to 115° C. for 20 minutes and 120° C. for 20 minutes. Once water ceased to collect in the Dean-Stark trap, the product was diluted with diethyl ether, collected via filtration over a short bed of silica, washed 4 times with saturated sodium bicarbonate, once with water and dried over magnesium sulfate. The diethyl ether was removed via rotary evaporation. Di-(2-methylbutyl)-DL-malate was obtained as a low viscosity, clear, very light yellow liquid with no detectable odor (139.8 g, 68% yield) after removing residual 2-methyl-1-butanol via vacuum distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06969738B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-25fe9aa8d82c485aa34ca7e716c6c7dc |
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| Source note | uspto-grants-2005_11 |
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