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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016181Generated: November 1, 2026

Ethyl 3-bromobenzoate → Ethyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoate

https://huagongshe.com/reaction/1016181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromobenzoateHCID 90488—
Reactant2-((Phenylmethoxy)methyl)-5-(tributylstannyl)-2H-tetrazoleHCID 11340561—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductEthyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoateHCID 57888757—

Reaction Steps

A solution of ethyl-3-bromobenzoate (0.47 g, 2.05 mmol) and 2-(benzyloxymethyl)-5-(tributylstannyl)-2H-tetrazole in toluene (20 mL) was degassed under vacuum and argon. To this solution was added copper (I) iodide (20 mg, 0.20 mmol) and tetrakis(triphenylphosphine)palladium(0) (115 mg, 0.10 mmol), and the mixture was again degassed under vacuum and argon. The flask and condenser were covered in foil to exclude light, and the reaction was heated at reflux temperature for 3 hours. After cooling to room temperature, the mixture was filtered and the filtrate was concentrated in-vacuo. The residue was purified over a 3.5×12 cm silica gel column, eluting with 5% then 10% then 15% ethyl acetate/hexanes to yield the title compound as a colorless oil which contained 5% of a tributyltin impurity. MS (ESI+)=339.22, (M+H)+. The oil was used as-is in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-84757f6997a64689b082e50bd6480972
Source noteuspto-grants-2011_07