HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857910Generated: October 31, 2026
Diethyl Ether → 4-(3-Nitrobenzyl)morpholine
https://huagongshe.com/reaction/857910
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(3-Nitrobenzyl)morpholine | HCID 783231 | — |
Reaction Steps
A solution of morpholine (4.57 mL) in toluene (10 mL) at 5° C. was treated with a solution of 3-nitrobenzyl chloride (4.29 g) in toluene (10 mL). After stirring at 85° C. for 2 hours the reaction mixture was allowed to cool to room temperature and then left to stand overnight. The reaction mixture was treated with diethyl ether (100 mL), then washed three times with water (50 mL), then three times with brine (50 mL), dried over magnesium sulfate and then evaporated. The residue was subjected to column chromatography on silica eluting with ethyl acetate to give the title compound (2.86 g) as a white solid, m.p. 48–50° C. 1H NMR [(CDCl3]: δ 8.24 (s, 1H), 8.13 (d, 1H), 7.70 (d, 1H), 7.50 (t, 1H), 3.74 (t, 4H), 3.60 (s, 2H) and 2.48 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07148215B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-c5f2422f441f4ad08cec5868cff11d31 |
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| Source note | uspto-grants-2006_12 |
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