HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720023Generated: October 31, 2026
Isopropanol → 1-(3-Chlorophenyl)cyclobutane-1-carbonitrile
https://huagongshe.com/reaction/720023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | m-Chlorophenylacetonitrile | HCID 73722 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(3-Chlorophenyl)cyclobutane-1-carbonitrile | HCID 21901979 | 71% |
Reaction Steps
A solution of 3.37 g (22.2 mmol) of 3-Chlorobenzyl cyanide and 4.93 g (24.4 mmol) of 1,3-dibromopropane in 15 mL of ether was added dropwise into 1.17 g (48.8 mmol) of NaH in 60 mL of DMSO. The temperature was held between 25° and 35° by water bath cooling. The mixture was stirred at room temperature for 18 hours. The mixture was cooled in ice water and 3 mL of 2-propanol was added dropwise, followed by the addition of 50 mL of water. The mixture was extracted with hexane (3×100 mL), and the combined extracts were washed with water (3×75 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated to yield 3.0 g (71%) product as colorless oil. 1H NMR (CDCl3) δ 2.04–2.16 (m, 1H), 2.38–2.50 (m, 1H), 2.56–2.67 (m, 2H), 2.79–2.89 (m, 2H), 7.29–7.36 (m, 3H), 7.41–7.43 (m, 1H). 13C NMR (CDCl3) 17.3, 34.8, 40.1, 124.2, 126.2, 128.4, 130.5, 135.2, 142.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132551B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-b3da49642a4b42d7a4485fadcd6467ef |
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| Source note | uspto-grants-2006_11 |
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