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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-bromobenzoate | HCID 90488 | — |
| Reactant | 2-((Phenylmethoxy)methyl)-5-(tributylstannyl)-2H-tetrazole | HCID 11340561 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985861B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-84757f6997a64689b082e50bd6480972 |
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| Source note | uspto-grants-2011_07 |
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