HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586813Generated: October 30, 2026
O-Xylene → 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)-2-(1-trityl-1H-tetrazol-5-yl)pyrrole
https://huagongshe.com/reaction/1586813
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | 4-Bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)pyrrole-2-carbonitrile | HCID 19759559 | — |
| Product | 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)-2-(1-trityl-1H-tetrazol-5-yl)pyrrole | HCID 19759467 | — |
Reaction Steps
A mixture of 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)pyrrole-2-carbonitrile (2.02 g) and trimethyltin azide (2.42 g) in xylene (20 ml) was stirred at 120° C. for 14 hours. After cooled to ambient temperature, the reaction mixture was concentrated in vacuo. To the residue was added trityl chloride (42 mg), triethylamine (50 μl) and methylene chloride (1 ml), and the mixture was treated in a conventional manner to give 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)-2-(1-trityl-1H-tetrazol-5-yl)pyrrole (1.63 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05215994 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-8a226c2ffee545b0b9679f04133daa7b |
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| Source note | uspto-grants-1993_06 |
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