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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761940Generated: October 31, 2026

Hydrochloric Acid → HCID 433777, compound

https://huagongshe.com/reaction/1761940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant4-Bromo-2-fluoro-1-(trifluoromethoxy)benzeneHCID 2782217—
ReactantMagnesiumHCID 5462224—
ReactantMethyl 2-(2H-tetrazol-2-yl)propanoateHCID 20042589—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 433777HCID 43377743.5%

Reaction Steps

Magnesium turnings (1.22 g) and iodine (1 crystal) were added to dry tetrahydrofuran (10 ml) under a nitrogen atmosphere. A solution of 3-fluoro-4-trifluoromethoxybromobenzene (12.95 g) in dry tetrahydrofuran (30 ml) was placed in a dropping funnel. About 10% of this was added to the mixture, and the Grignard reaction began immediately. The rest of the mixture was added dropwise with stirring, and the temperature rose until the solvent was at reflux. After the addition was complete the mixture was allowed to cool, then a solution of methyl-2-(2H-tetrazol-2-yl)propionate (3.9 g) in dry tetrahydrofuran (10 ml) was added with stirring. An exotherm was noted, and the reaction was allowed to stir at room temperature for 30 minutes. The mixture was then poured into water (100 ml). The mixture was acidified by adding 3M hydrochloric acid (100 ml) and then extracted with diethyl ether (3×100 ml). The combined ethereal extracts were dried over anhydrous sodium sulphate and evaporated to a brown oil (10 g). This was chromatographed on silica gel eluting with 4:1 hexane/ethylacetate to give an oil (1.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04829074
Source datasetuspto-grants-1989_05
ORD IDord-1880e1dc11c34a4d82ef539c375337b5
Source noteuspto-grants-1989_05