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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099146Generated: November 1, 2026

Diiodomethane → 4-(1-Methylcyclopropyl)phenol

https://huagongshe.com/reaction/2099146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 21898100HCID 21898100—
ReactantHCID 178418750HCID 178418750—
Solvent1,1-DichloroethaneHCID 6365—
Product4-(1-Methylcyclopropyl)phenolHCID 1797304768%

Reaction Steps

Diethylzinc (1.0 M in hexanes, 69 mL, 69 mmol) was added to a solution of tert-butyl-(4-isopropenyl-phenoxy)-dimethyl-silane (6.85 g, 27.6 mmol) in dichloroethane at 0° C. Diiodomethane (11.2 mL, 138 mmol) was then added dropwise to the solution and the resultant mixture was stirred at 0° C. for 0.5 h and allowed to warm to rt for 2 h. The opaque mixture was quenched with saturated aqueous NH4Cl. The aqueous phase was extracted with CH2Cl2 and the combined organic layers were washed with saturated aqueous NaHCO3. The organic layers were dried over sodium sulfate, filtered through celite, and concentrated. The crude TBS ether was dissolved in THF (50 mL) and TBAF (1.0 M in THF, 28 mL, 28 mmol) was added at rt. The solution was stirred for 2 h and then quenched with aqueous 1.0 M HCl. The aqueous phase was extracted with ethyl acetate and the combined organic layers were washed with saturated NaHCO3. The organic layers were dried over sodium sulfate, filtered and concentrated. Purification by silica-gel chromatography (1% 2-propanol/12% ethyl acetate in hexanes) provided 4-(1-methyl-cyclopropyl)-phenol (2.77 g, 68%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569568B2
Source datasetuspto-grants-2009_08
ORD IDord-5c19c613203a404eabf271a87ab00192
Source noteuspto-grants-2009_08