HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377203Generated: November 1, 2026
Trimethylsilyl iodide → Methyl 5-tert-butyl-6-hydroxy-4'-methyl-3-biphenylcarboxylate
https://huagongshe.com/reaction/2377203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Methyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylate | HCID 12084817 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 5-tert-butyl-6-hydroxy-4'-methyl-3-biphenylcarboxylate | HCID 12084822 | 36% |
Reaction Steps
5.4 g (14 mmol) of methyl 6-benzyloxy-5-tert-butyl-4′-methyl-3-biphenylcarboxylate (Example 1, d) are dissolved in 100 mL of acetonitrile. 6 mL (41 mmol) of trimethylsilyl iodide are added and the mixture is heated at 50° C. for 24 hours. After extraction, the residue obtained is subjected to esterification conditions similar to those of Example 1 b, and the residue obtained is purified by chromatography. A white solid is obtained (m=1.6 g, yield=36%; m.p.=105° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468457B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-350307f600c54d5bae5d5afcc5fad76e |
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| Source note | uspto-grants-2008_12 |
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