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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371536Generated: October 25, 2026

2,3,5-Trimethylphenol → 2,3,5-Trimethylphenyl isopropyl ether

https://huagongshe.com/reaction/371536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,5-TrimethylphenolHCID 12769—
Reactant4-Isopropoxy-2,3,6-trimethyl-benzyl-triphenylphosphonium chlorideHCID 86735903—
Product2,3,5-Trimethylphenyl isopropyl etherHCID 20210001—

Reaction Steps

The 4-isopropoxy-2,3,6-trimethyl-benzyl-triphenylphosphonium chloride employed as the starting material is prepared by the procedure described in Example 18 by alkylation of 2,3,5-trimethylphenol to give 2,3,5-trimethylphenyl isopropyl ether (boiling point 115° C./11 mmHg), by haloformylation of the ether obtained to give 4-isopropoxy-2,3,6-trimethyl-benzyl chloride (nD20 =1.5433) and by reaction of the latter compound with triphenylphosphine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04532355
Source datasetuspto-grants-1985_07
ORD IDord-88b398c8fb374ae09fa937ef08d13332
Source noteuspto-grants-1985_07