HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377800Generated: October 26, 2026
Sodium hydride → Ethyl 5-cyano-5-(3,4-dichlorophenyl)pentanoate
https://huagongshe.com/reaction/377800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | (3,4-Dichlorophenyl)acetonitrile | HCID 76690 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-cyano-5-(3,4-dichlorophenyl)pentanoate | HCID 22741808 | 45.8% |
Reaction Steps
11.8 g of a 55% dispersion of sodium hydride in oil are suspended in 100 ml of THF and cooled in an ice bath, a solution of 50 g of 3,4-dichlorophenylacetonitrile in 50 ml of THF is added dropwise and the reaction mixture is stirred for 3 hours at RT. It is cooled again in an ice bath, a solution of 52.4 g of ethyl 4-bromobutanoate in 50 ml of THF is added dropwise and the mixture is stirred overnight at RT. It is concentrated under vacuum, the residue is taken up with water and extracted with ether, the organic phase is washed with water, with a buffer solution of pH 2, with water and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using toluene and then a toluene/AcOEt mixture (100/5; v/v) as the eluent to give 36.9 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06028082 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-02387f9c4eb64c1f8e59cf5ee705b21b |
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| Source note | uspto-grants-2000_02 |
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