HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223464Generated: October 25, 2026
1,3-Dibromopropane → 1-(4-Chlorophenyl)cyclobutanecarbonitrile
https://huagongshe.com/reaction/223464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chlorobenzyl cyanide | HCID 241582 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(4-Chlorophenyl)cyclobutanecarbonitrile | HCID 98621 | 85.4% |
Reaction Steps
4-Chlorobenzyl cyanide (10 g) in dry DMSO (20 ml) was added over 5 min to a stirred suspension of sodium hydride (4.4 g) in DMSO at 25° C. under argon. The mixture was stirred for 30 minutes then a solution of 1,3-dibromopropane (27 g) in dry DMSO (50 ml) was added over 30 minutes while maintaining the temperature of the reaction mixture at 25°-30° C. After stirring an additional 40 minutes at this temperature the reaction mixture was added to ice water (500 ml) and extracted with dichloromethane (3×75 ml). The extracts were evaporated and the residue extracted with diethyl ether (4×50 ml). The ether extracts were washed with water, dried over anhydrous sodium sulphate and evaporated to yield an oil (10.8 g) which on distillation gave the nitrile [bp 90°/10-6Torr.] yield 5.4 g (43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04355042 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-be96759ba097479885748c985dc5144a |
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| Source note | uspto-grants-1982_10 |
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