HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608227Generated: October 31, 2026
Hydrazine hydrate (1:1) → 2-Acetylaminomethyl-4-(2-chlorobenzyl)-6-methylmorpholine
https://huagongshe.com/reaction/1608227
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[[4-(2-chlorobenzyl)-6-methyl-2-morpholinyl]methyl]phthalimide | HCID 19848602 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Acetylaminomethyl-4-(2-chlorobenzyl)-6-methylmorpholine | HCID 19848604 | 74.8% |
Reaction Steps
A mixture of N-[[4-(2-chlorobenzyl)-6-methyl-2-morpholinyl]methyl]phthalimide (26 g), 100% hydrazine hydrate (4.2 g), and ethanol (20 ml) is refluxed with stirring for 15 minutes. After the insoluble materials are filtered off, the filtrate is diluted with water and extracted with chloroform. The organic layer is washed successively with water and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and filtered. Acetic anhydride (14.7 g) is added to the filtrate, and the mixture is stirred at 25° C. for 2 hours. The reaction mixture is washed successively with aqueous sodium hydroxide solution, water and saturated aqueous sodium chloride solution, and dried over magnesium sulfate. After removal of the solvent under reduced pressure, the residue is chromatographed on silica gel with ethyl acetate to give the title compound (15 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04870074 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-cb198b78b670468b8f21b25adda362c3 |
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| Source note | uspto-grants-1989_09 |
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