HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971913Generated: October 28, 2026
Diisopropylamine → 1,4-Bis(2-carbomethoxy-2-methylpropyl)benzene
https://huagongshe.com/reaction/971913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methyl isobutyrate | HCID 11039 | — |
| Reactant | 1,4-Bis(bromomethyl)benzene | HCID 69335 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1,4-Bis(2-carbomethoxy-2-methylpropyl)benzene | HCID 21312576 | 86.1% |
Reaction Steps
To 1 liter of dry tetrahydrofuran was added 52 g of diisopropylamine. The mixture was cooled to -78° C. and 325 ml of 1.6 M n-butyllithium in hexane was added. After 1 hour of stirring 52 g of methyl isobutyrate was added dropwise followed by stirring for another 30 minutes. Then 63 g of α,α'-dibromo-p-xylene was slowly added. The reaction mixture was stirred overnight and brought to room temperature. The mixture was filtered and solvent was removed from the filtrate by evaporation. The residue was recrystallized from methanol to obtain 63 g of 1,4-bis(2-carbomethoxy-2-methylpropyl)benzene, m.p. 74°-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04161607 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-a8576a09ff17453b896866f76c58a23f |
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| Source note | uspto-grants-1979_07 |
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