HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Diethyl (4-chlorobutyl)propanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl (4-chlorobutyl)propanedioate | HCID 53401795 | 32% |
Reaction Steps
To 458 ml of dry tetrahydrofuran (THF) was added 13.4 g of 60% sodium hydride, and 160.6 g of diethyl malonate was added dropwise with stirring under ice-cooling. After addition, stirring was continued for 15 minutes, and 57.3 g of 1-bromo-4-chlorobutane was added. The mixture was stirred for 50 hours at room temperature. The reaction solution was poured into ice-cold water, neutralized with dilute hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated. The residue was distilled under reduced pressure to provide 26.8 g of the objective compound as colorless oil. B.p. 127–130° C. (5 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998412B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-433648082b664057b51bf62d4090cdee |
| Source note | uspto-grants-2006_02 |