HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376107Generated: October 27, 2026
Acetic Acid → 6-(N-benzyloxycarbonylamino)-2-methylene-hexanal
https://huagongshe.com/reaction/376107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Benzyl 6-oxohexylcarbamate | HCID 11391023 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(N-benzyloxycarbonylamino)-2-methylene-hexanal | HCID 18991505 | — |
Reaction Steps
2.44 g (30 mmol) of 37% aqueous formaldehyde solution are added to a solution of 1.5 g (17 mmol) of anhydrous piperazine and 2.03 g (34 mmol) of acetic acid in 18.7 ml of water. The mixture is stirred at 25° for 15 minutes, and then 7.48 g (30 mmol) of 6-(N-benzyloxycarbonylamino)hexanal are added thereto. The reaction mixture is heated under reflux for 2 hours and then cooled with ice-water and extracted twice with 50 ml of methylene chloride each time. The extracts are combined, washed twice with 25 ml of saturated sodium hydrogen carbonate solution each time and with 25 ml of saturated sodium chloride solution, dried and concentrated to dryness by evaporation. 6-(N-benzyloxycarbonylamino)-2-methylene-hexanal is obtained in the form of a yellowish liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05488140 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-83d43faa82ea4c958bfe346f32f4199a |
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| Source note | uspto-grants-1996_01 |
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