HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103728Generated: October 30, 2026
N-(4-cyanophenyl)acetamide → HCID 69058617, compound
https://huagongshe.com/reaction/2103728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(4-cyanophenyl)acetamide | HCID 37256 | — |
| Reactant | 1-Chloro-4-iodobutane | HCID 82527 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 69058617 | HCID 69058617 | — |
Reaction Steps
9 g (54.1 mmol) of N-(4-cyanophenyl)acetamide are dissolved in 100 ml of THF. The mixture is cooled to 0° C. before the dropwise addition of 51 ml of a 1.6 N solution in hexane of nBuLi (1.5 eq.). The solution is left for one hour to return to ambient temperature and is then cooled to 0° C. before the dropwise addition of 9.9 ml of 1-chloro-4-iodobutane (81 mmol). The reaction mixture is stirred at ambient temperature for 18 h and then hydrolysed with a saturated aqueous solution of ammonium chloride (100 ml) and extracted with ethyl acetate. The organic phases are combined, dried over magnesium sulphate and concentrated. Purification by chromatography on silica (eluant: petroleum ether/ethyl acetate: 1/1) yields a yellow oil containing the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576120B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-a18af5e5e0c34bc6afafaff429a11712 |
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| Source note | uspto-grants-2009_08 |
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