HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612795Generated: October 31, 2026
Benzonitrile, 2-(3,4-dichlorophenoxy)- → HCID 19926666, compound
https://huagongshe.com/reaction/1612795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzonitrile, 2-(3,4-dichlorophenoxy)- | HCID 514863 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19926666 | HCID 19926666 | 75% |
Reaction Steps
A solution of 10 g of anhydrous aluminum chloride in 150 ml of dry diethyl ether was added dropwise under nitrogen to a suspension of 3.1 g of lithium aluminum hydride in 150 ml of dry diethyl ether, and the mixture was cooled at 0° C. After 30 min at 0° C., a solution of 5.0 g of 2-(3,4-dichlorophenoxy)benzonitrile in 150 ml of dry diethyl ether was added slowly. The mixture was stirred for 24 h at 25° C., and a concentrated aqueous solution of sodium hydrogen carbonate was added. The precipitate was filtered off, the filtrate was evaporated to dryness, dissolved in ethyl acetate, and acidified with a concentrated solution of hydrochloric acid in ethanol. The precipitate was collected and recrystallized from a mixture of ethanol and diethyl ether, to give in 75% yield 2-(3,4-dichlorophenoxy)benzenemethanamine hydrochloride. mp 213° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05190965 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-56d8f63501e34337863efb1030ad59e9 |
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| Source note | uspto-grants-1993_03 |
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