HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370853Generated: October 30, 2026
Hydrochloric Acid → HCID 13477628, compound
https://huagongshe.com/reaction/370853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13477606 | HCID 13477606 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13477628 | HCID 13477628 | 64% |
Reaction Steps
To a degreased suspension of sodium hydride (23 g) in tetrahydrofuran at ice temperature is slowly added (under nitrogen) a solution of 3-[(4-acetyl-3-hydroxyphenoxy)methyl]nitrobenzene (13.6 g, prepared as in Example 1A) in tetrahydrofuran (100 ml). When hydrogen evolution ceases, the mixture is allowed to warm to room temperature and is stirred for 2 hours. To this slurry is added iodomethane (6.7 g, neat) and the mixture is stirred 15 hours at room temperature. Another 6.7 g of iodomethane is then added and the mixture is refluxed 6 hours. After cooling to room temperature, the reaction mixture is poured into 10% HCl and extracted with ether. The extracts are washed with saturated brine, then dried over MgSO4 and concentrated. Recrystallization from acetone gives 9.1 g (64% yield) of product, m.p. 111°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04528392 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-42c5bab7e0224d168838a284ecb7d6de |
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| Source note | uspto-grants-1985_07 |
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