HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099146Generated: November 1, 2026
Diiodomethane → 4-(1-Methylcyclopropyl)phenol
https://huagongshe.com/reaction/2099146
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 21898100 | HCID 21898100 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-(1-Methylcyclopropyl)phenol | HCID 17973047 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569568B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-5c19c613203a404eabf271a87ab00192 |
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| Source note | uspto-grants-2009_08 |
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