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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452562Generated: October 27, 2026

Hydrochloric Acid → [3-(dimethylamino)phenyl](1-methyl-1H-tetrazol-5-yl)methanone

https://huagongshe.com/reaction/452562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1H-Tetrazole, 1-methyl-HCID 140123—
Reactant3-(dimethylamino)-N-methoxy-N-methylbenzamideHCID 45794498—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product[3-(dimethylamino)phenyl](1-methyl-1H-tetrazol-5-yl)methanoneHCID 6707508525%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 1-methyl-1H-tetrazole (4.54 g, 54 mmol) in anhydrous THF (200 mL), cooled to 0° C. with a brine/ice bath, was added dropwise a solution of isopropylmagnesium chloride (2 M in THF, 27 mL, 54 mmol). After the addition was over, the resulting cloudy suspension was stirred for 15 min at 0° C. A solution of 3-(dimethylamino)-N-methoxy-N-methylbenzamide (9.37 g, 45 mmol) in THF (80 mL) was then added dropwise while keeping the internal temperature below 5° C. The reaction mixture was then allowed to warm up and stirred at room temperature for 1 h. A mixture of ice-cold water (50 mL) and aq. HCl (1 M, 55 mL) was added to the reaction mixture, the layers were separated, the water phase was extracted with ethyl acetate (3×50 mL) and the combined organic layers were dried. Purification on silica gel followed by recrystallization from diethyl ether afforded [3-(dimethylamino)phenyl](1-methyl-1H-tetrazol-5-yl)methanone as a bright yellow solid [3.06 g, yield 25%; HPLC/MS:m/z=232 (M+H); log P(HCOOH)=2.21].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492388B2
Source datasetuspto-grants-2013_07
ORD IDord-d7e27ec61ad5410f875267ddb006d8fe
Source noteuspto-grants-2013_07