HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108076Generated: October 30, 2026
2-Methylbenzoic acid → 2-dodecylbenzoic Acid
https://huagongshe.com/reaction/2108076
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylbenzoic acid | HCID 8373 | — |
| Reactant | 1-Bromoundecane | HCID 12744 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-dodecylbenzoic Acid | HCID 122418 | — |
Reaction Steps
A solution containing lithium diisopropylamide (0.1 mole) was prepared by treating a solution of dissopropylamine (14.1 ml, 0.1 mole) in tetrahydrofuran (200 ml) at 0° C. with n-butyl lithium (41.2 ml of a 2.43 M solution, 0.1 mole), and stirring for 5 minutes. To this was added a solution of o-toluic acid (6.8 g, 0.05 mole) in tetrahydrofuran (50 ml). The ice bath was removed and the intense red solution was stirred for 30 minutes. This solution was slowly pipetted into a solution of undecylbromide (11.8 g, 0.05 mole) in tetrahydrofuran (50 ml) at -20° C. After the addition, the cooling bath was removed and the solution stirred for 30 minutes. A small amount of water was added and most of the tetrahydrofuran was removed under reduced pressure. The residue was poured into water, acidified with 3N hydrochloric acid and extracted with ether. The ether was dried, evaporated and the residue was recrystallized from acetonitrile, then from hexane, to give the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04937253 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-b9fdf90f8f554d6bb45c1e044427c46a |
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| Source note | uspto-grants-1990_06 |
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