HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936730Generated: October 30, 2026
Diisopropylethylamine → HCID 18519986, compound
https://huagongshe.com/reaction/1936730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 2,6-Cycloheptadien-1-one | HCID 10920463 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 18519986 | HCID 18519986 | 20% |
Reaction Steps
N,N-Diisoproylethylamine (14.5 ml) was added dropwise to a stirred suspension of O-methylhydroxylamine hydrochloride (2.32 g) in isopropyl alcohol (25 ml). After 30 minutes cyclohepta-2,6-dienone (3.0 g) in isopropyl alcohol (5 ml) was added dropwise. After 24 hours N,N-diisopropylethylamine (4.9 ml) was added. After 6 hours the mixture was allowed to stand at room temperature overnight. The mixture was evaporated under reduced pressure, diethyl ether added and the resulting mixture extracted with 2M hydrochloric acid (x3). The combined aqueous fractions were washed with diethyl ether (x3), neutralised with sodium hydroxide and extracted with diethyl ether (x3). The combined extracts were washed with brine, dried (MgSO4) and evaporated under reduced pressure. Kugelrohr distillation gave 8-methoxy-8-azabicyclo[3.2.1]octan-3-one (0.86 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391883B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-4c8e9ae7457343029b6921c0978c78ca |
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| Source note | uspto-grants-2002_05 |
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