HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916700Generated: October 27, 2026
Dimethylformamide → 2-(4-Iodo-2-methyl-phenoxy)-ethanol
https://huagongshe.com/reaction/1916700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Iodo-2-methylphenol | HCID 143713 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Iodo-2-methyl-phenoxy)-ethanol | HCID 4055115 | — |
Reaction Steps
Under an N2 atmosphere 2.34 g (10 mmol) 4-iodo-2-methyl-phenol are added to a suspension batchwise, cooled to 0° C., of 0.48 g (11 mmol) NaH in 50 mL THF and stirred for a further 30 min at this temperature. Then 0.85 mL (12 mmol) 2-bromoethanol, dissolved in 5 mL THF, are added dropwise and the mixture is stirred for 18 h at RT. 5 mL of DMF are added and the reaction mixture is heated to 70° C. for 8 h. The mixture is evaporated down i. vac., the residue is taken up in water, extracted exhaustively with EtOAc and dried with Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography on silica gel (cyc/EtOAc 7:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618132B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-c18045f3f9bb47009f91f4ff3b733bee |
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| Source note | uspto-grants-2013_12 |
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