HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278860Generated: November 3, 2026
Water → 2-[3-(2-Morpholin-4-ylethoxy)phenyl]acetonitrile
https://huagongshe.com/reaction/1278860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Methyl 3-(2-morpholin-4-ylethoxy)benzoate | HCID 7164628 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| Product | 2-[3-(2-Morpholin-4-ylethoxy)phenyl]acetonitrile | HCID 22262779 | — |
Reaction Steps
Lithium diisopropylarmide (18.8 ml, 37 mmol, 2.0 M solution in heptane/tetrahydrofuran/ethylbenzene) was added dropwise to a solution of acetonitrile (1.58 g, 37 mmol) in dry tetrahydrofuran (50 ml) at −78° C. After stirring the reaction mixture for 30 min., a solution of methyl 3-(2-morpholin-4-ylethoxy)benzoate in dry tetrahydrofuran (50 ml) was added dropwise over 10 min. After 15 min., water was added and the reaction mixture was allowed to warm to room temperature. The aqueous layer was separated and acidified with dilute hydrochloric acid to pH 7. The product was extracted into ethyl acetate and washed with water and brine and dried over magnesium sulfate. The organics were removed in vacuo to give 2-[3-(2-morpholin-4-ylethoxy)phenyl]acetonitrile (5.0 g) as an oil which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06444696B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-b5003a2ef39544948c8e990cb813884a |
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| Source note | uspto-grants-2002_09 |
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