HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389246Generated: October 30, 2026
Hydrochloric Acid → 7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane
https://huagongshe.com/reaction/389246
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Benzyl-7-t-butoxycarbonylamino-4-oxo-7-methyl-5-azaspiro[2.4]heptane | HCID 57758653 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane | HCID 57587306 | 90.2% |
Reaction Steps
5-Benzyl-7-t-butoxycarbonylamino-4-oxo-7-methyl-5-azaspiro[2.4]heptane (43.63 g) was dissolved in toluene, and the solution was stirred under ice-cooling. 37% Concentrated hydrochloric acid (100 mL) was added dropwise thereto, followed by stirring. After 0.5 hours, water was added to the reaction mixture. The mixture was stirred and left to stand so as to separate the aqueous layer from the organic layer. Sodium hydroxide (54 g) was added to and dissolved in the separated aqueous layer so as to alkalify the layer. The aqueous layer was extracted several times with toluene repeatedly. All the toluene layers were combined and washed with saturated brine. The washed toluene layer was dried with sodium sulfate, followed by filtration. The filtrate was concentrated under reduced pressure, to thereby yield the title product (21.29 g, yield: 90.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378119B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-0f92f70949fc405fa759941366ac1f4e |
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| Source note | uspto-grants-2013_02 |
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