HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236489Generated: October 30, 2026
Diisopropylamine → 4-Tert-butyl-2-(carboxymethyl)benzoic acid
https://huagongshe.com/reaction/2236489
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | 4-Tert-butyl-2-methylbenzoic acid | HCID 11958977 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Tert-butyl-2-(carboxymethyl)benzoic acid | HCID 42625830 | — |
Reaction Steps
To a magnetically stirred solution of diisopropyl amine (0.75 g, 7.4 mmol) in THF (5 mL) at −30° C. is added BuLi (3.4 mL, 2.5 M in hexanes, 8.5 mmol). The mixture is stirred for 10 minutes at this temperature and cooled to −78° C. A solution of 4-tert-Butyl-2-methyl-benzoic acid [J. Am. Chem. Soc. 1944, 66, 154] (250 mg, 1.3 mmol) and dimethylcarbonate (150 mg, 1.67 mmol) in THF (3 mL) is added dropwise at −78° C. The mixture is allowed to stir at this temperature for 2 hours before it is allowed to warm to room temperature. The mixture is quenched with MeOH and water once it reached room temperature. After removal of THF, the water layer is extracted with ether. The water layer is acidified with HCl and the product is extracted from ether. After chromatography, the title compound is isolated pure (125 mg, 41%). MS (ESI): 237.1 (M+1)+1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713994B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-f601c3286c17427caa1a2505a2a7ef38 |
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| Source note | uspto-grants-2010_05 |
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