HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745935Generated: October 30, 2026
Hydrochloric Acid → HCID 23311107, compound
https://huagongshe.com/reaction/745935
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 5-Methylisoxazole | HCID 79833 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 67709229 | HCID 67709229 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23311107 | HCID 23311107 | 29% |
Reaction Steps
To a solution of lithium diisopropylamide (LDA), prepared from n-BuLi (64.5 ml, 0.1M) and diisopropylamine (10.1 g, 14 ml, 0.1M) in dry THF (100 ml) was added under N2 at -10° C. 5-methylisoxazole (4.2 g, 4.1 ml, 0.05M). The resultant yellow suspension was stirred (mechanical stirrer) at -10° C. for 1 hr before 1-aza-2-methoxy-1-cyclohexene (5.6 g, 0.05M) was added dropwise. A light yellow precipitate was immediately formed. The mixture was allowed to warm to ambient over a period of 20 hr. MeOH (40 ml) was slowly added and the resulting reddish solution was stirred at ambient for 2 hr. The solvents were evaporated in vacuo, and the residual oil was flash column chromatographed on silica gel (EM-60) with 30% MeOH in CH2Cl2 as the eluent to give the desired free base. The HCl salt was then prepared by adding conc HCl to a solution of the free base in methanol. Recrystallization from MeOH/ether gave the title compound (2.9 g, 29%). TLC (30% MeOH in CH2Cl2); Rf=0.53. IR (KBr), cm-1, 3330, 3180, 3030, 2950.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04602013 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-a985bc560616415d9907e3ed1a85ae40 |
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| Source note | uspto-grants-1986_07 |
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