HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354732Generated: October 30, 2026
2-Bromopropane → 2-(4-Methoxyphenyl)-3-methylbutyronitrile
https://huagongshe.com/reaction/354732
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Benzeneacetonitrile, 4-methoxy- | HCID 66031 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Methoxyphenyl)-3-methylbutyronitrile | HCID 13059056 | 99.1% |
Reaction Steps
To a stirred suspension of sodium hydroxide pels (320.0 g; 8.0 mol) in isopropyl bromide (492.0 g; 4.0 mol) is added 4-methoxyphenylacetonitrile (294.3 g; 2.0 mol) over a 30-minute period at a temperature of 50°-55° C. Following this addition the reaction mixture is stirred at reflux (68°-74° C.) for 4 hours. It is then cooled to 50° C. and water (498 ml) is added. The mixture is subsequently stirred for 15 minutes with cooling. The aqueous and organic phases are then separated and the excess isopropyl bromide is removed from the organic phase by distillation. The resulting product (367.88 g of 2-(4-methoxyphenyl)-3-methylbutyronitrile) is 96.9% pure and corresponds to a real yield of 99.1%. The results of this experiment are included in Table Ia under No. 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377531 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-a95bcfc508da40b5a4f025acd32c0c2b |
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| Source note | uspto-grants-1983_03 |
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