HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520299Generated: November 3, 2026
N,N,N',N'-Tetramethyl-1,3-diaminopropane → Methyl 4-((1-(4-bromo-2-methylphenyl)-2-methylpropyl)amino)benzoate
https://huagongshe.com/reaction/1520299
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethyl-1,3-diaminopropane | HCID 8084 | — |
| Reactant | Methyl 4-aminobenzoate | HCID 12082 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(4-Bromo-2-methylphenyl)-2-methylpropan-1-ol | HCID 115840179 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-((1-(4-bromo-2-methylphenyl)-2-methylpropyl)amino)benzoate | HCID 117840512 | 49.3% |
Reaction Steps
To a mixture of 1-(4-bromo-2-methylphenyl)-2-methylpropan-1-ol (600 mg), N,N,N′,N′-tetramethyl-1,3-propanediamine (0.492 mL) and toluene (0.823 mL) was added methanesulfonyl chloride (0.229 mL), and the mixture was stirred at 60° C. for 2 hr. To the reaction mixture were added methyl 4-aminobenzoate (560 mg) and N,N-diisopropylethylamine (0.862 mL) at room temperature, and the mixture was stirred at 100° C. overnight under a nitrogen atmosphere. To the reaction mixture was added water at room temperature, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (457.4 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073864B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-18bfe7efb3b74d868b7305481b16d707 |
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| Source note | uspto-grants-2015_07 |
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