HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249176Generated: November 1, 2026
Methoxyacetic Acid → HCID 70454348, compound
https://huagongshe.com/reaction/1249176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Didesmethylsibutramine | HCID 134772 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 70454348 | HCID 70454348 | — |
Reaction Steps
Sodium borohydride (2.5 g) was added portionwise to a stirred solution of methoxyacetic acid (26.4 g) in toluene (300 ml) under an atmosphere of nitrogen and stirring was continued for 16 hours. A solution of 1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutylamine (5 g) in toluene (50 ml) was then added and the mixture was heated under reflux with stirring for 24 hours. After cooling the reaction mixture, water (200 ml) was added and the mixture was basified with 16N aqueous sodium hydroxide solution. The product was extracted into ether and the extracts were washed with water, dried and evaporated to give a brown oil which was dissolved in ether (30 ml). A solution of maleic acid (4.8 g) in ether (250 ml) was added. The solid which precipitated was collected, dried and recrystallised from ethyl acetate with hot filtering to give N-(2-methoxyethyl)-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutylamine maleate (m.p. 131°-133° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04629727 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-f21880ca2c794884b34b0a0020fce694 |
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| Source note | uspto-grants-1986_12 |
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