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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089552Generated: October 29, 2026

Hydrochloric Acid → HCID 59199437, compound

https://huagongshe.com/reaction/2089552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphineHCID 11776—
Reactant1,4-DioxaneHCID 31275—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantHCID 59199372HCID 59199372—
ReactantHCID 178418785HCID 178418785—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59199437HCID 59199437—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of acetic acid 4-chloro-3-hydroxy-2,2-dimethyl-indan-1-yl ester (1.55 g, 6.1 mmol) in THF (30 mL) is added methyl 4-imidazolecarboxylate (CAS#17325-26-7, 1.53 g, 12.2 mmol), and triphenylphosphine (3.2 g, 12.2 mmol). The reaction is cooled to 0° C. and di-t-butyl azodicarboxylate (2.81 g, 12.2 mmol) is added. The reaction is placed at room temperature and permitted to stir for ca. 12 hours and then is heated to 40° C. for 1.5 hours. The reaction mixture is cooled to 0° C., quenched with 4 N HCl in dioxane (20 mL, 80 mmol), and stirred for 30 minutes. The reaction is concentrated to near dryness and diluted with ethyl acetate. The organic layer is extracted three times with 1 N aqueous HCl. The aqueous extracts are combined, neutralized with Na2CO3, and extracted three times with ethyl acetate. The combined organic layers are dried with Na2SO4, filtered, and concentrated. The resulting residue is purified by silica gel flash chromatography (ethyl acetate-dichloromethane, 0:1 to 1:3) to furnish 3-(3-acetoxy-7-chloro-2,2-dimethyl-indan-1-yl)-3H-imidazole-4-carboxylic acid methyl ester; MS: (ESI) m/z 332.04 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436035B2
Source datasetuspto-grants-2013_05
ORD IDord-7fc4fbb775ee46c2b1bc106188dd80b9
Source noteuspto-grants-2013_05