HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79498Erstellt: 24. Oktober 2026
Diisopropylamine → 4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate
https://huagongshe.com/de/reaction/79498
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | tert-Butyl bromoacetate | HCID 79177 | — |
| Edukt | Methyl 3-(4-chlorophenyl)propanoate | HCID 8027172 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate | HCID 68733696 | 81,4% |
Reaktionsschritte
BuLi (5.2 mL, 1.6M in hexanes) was added to a 0° C. solution of diisopropylamine (0.91 g, 9.0 mmol) in THF (40 mL). The reaction mixture was then stirred at 0° C. for 30 minutes, and then cooled to −78° C. A solution of methyl 3-(4-chlorophenyl)propanoate (1.5 g, 7.5 mmol) in THF (8 mL) was added slowly, and the reaction mixture was stirred at −78° C. for 40 minutes. A solution tert-butyl 2-bromoacetate (4.4 g, 22.7 mmol) in THF (5 mL) was then added. The reaction was then stirred for 30 minutes at −78° C. and then warmed to room temperature and stirred overnight. The reaction was then quenched with saturated NH4Cl and concentrated to remove THF. The reaction was then extracted with EtOAc, and the combined extracts were dried (Na2SO4), filtered, concentrated, and dried in vacuo to give 4-tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate (1.91 g, 81%) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841304B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-6674fe9f14df488cbb58d62056c61ab6 |
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| Quellennotiz | uspto-grants-2014_09 |
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