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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745935Generated: October 30, 2026

Hydrochloric Acid → HCID 23311107, compound

https://huagongshe.com/reaction/745935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
Reactant5-MethylisoxazoleHCID 79833—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 67709229HCID 67709229—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23311107HCID 2331110729%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04602013
Source datasetuspto-grants-1986_07
ORD IDord-a985bc560616415d9907e3ed1a85ae40
Source noteuspto-grants-1986_07