HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706526Generated: October 31, 2026
Methanol → 3-Amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone
https://huagongshe.com/reaction/1706526
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | HCID 23463638 | HCID 23463638 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone | HCID 53965487 | 82.6% |
Reaction Steps
3-Phthalimido-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone (1.90 g.) and N,N-dimethyl-1,3-propanediamine (1.14 g.) were added to a mixture of methanol (20 ml.) and chloroform (5 ml.), whereafter the mixture was stirred at ambient temperature for 17 hours. The reaction mixture was evaporated to dryness under reduced pressure to give a residue, which was dissolved in ethyl acetate (20 ml.). The solution was extracted with three portions of an aqueous solution consisting of 1 N hydrochloric acid (5.3 ml.) and water (11.3 ml.), and then the combined extract was washed with ethyl acetate. The aqueous solution was adjusted to pH 8 with sodium bicarbonate under ice-cooling and then extracted with three 10 ml. portions of chloroform. The extracts were washed with water and then dried over magnesium sulfate. The solvent was removed by distillation from the solution under reduced pressure to give oily 3-amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone (1.030 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04207234 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-67c3f9330db54dec966e098c979dc729 |
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| Source note | uspto-grants-1980_06 |
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