HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172385Generated: October 25, 2026
Toluene → 2-Formyl-2,5-dimethyl-hexanoic acid ethyl ester
https://huagongshe.com/reaction/1172385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Diethyl 2-Isopentyl-2-methylmalonate | HCID 233614 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Formyl-2,5-dimethyl-hexanoic acid ethyl ester | HCID 57446163 | 36.5% |
Reaction Steps
A solution of 2-methyl-2-(3-methyl-butyl)-malonic acid diethyl ester (500 mg, 2.05 mmol) in anhydrous dichloromethane (4 mL) was stirred at −78° C. under a blanket of nitrogen and treated dropwise via syringe with a 1.0 M solution of DIBAL in toluene (4.1 mL, 4.1 mmol) over a period of 15 min. The reaction was stirred for 4 h at −78° C. and quenched sequentially with a saturated aqueous ammonium chloride solution (3 mL) and a 4% aqueous hydrochloric acid solution (3 mL). The resulting gelatinous suspension was allowed to warm to 25° C. and was filtered through a sintered glass funnel. The filtrate was concentrated in vacuo. The resulting crude oil was purified by flash column chromatography (ISCO RediSep column, 0 to 20% ethyl acetate in hexanes) to give 2-formyl-2,5-dimethyl-hexanoic acid ethyl ester (150 mg, 36%) as a clear oil. 1H NMR (400 MHz, CDCl3) δ: 0.89 (d, 6H, J=6.9 Hz), 1.07-1.15 (m, 2H), 1.23-1.26 (m, 3H), 1.28 (s, 3H), 1.52 (septet, 1H, J=6.6 Hz), 1.83-1.92 (m, 2H), 4.21 (q, 2H, J=6.9 Hz), 9.69 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834009B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-45543097277e48fe882891922c3f9ddc |
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| Source note | uspto-grants-2010_11 |
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