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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantMethyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylateHCID 12084817—
SolventAcetonitrileHCID 6342—
ProductMethyl 5-tert-butyl-6-hydroxy-4'-methyl-3-biphenylcarboxylateHCID 1208482236%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468457B2
Source datasetuspto-grants-2008_12
ORD IDord-350307f600c54d5bae5d5afcc5fad76e
Source noteuspto-grants-2008_12