HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704069Generated: October 30, 2026
4-tert-Butylphenol → HCID 12531881, compound
https://huagongshe.com/reaction/1704069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20392570 | HCID 20392570 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12531881 | HCID 12531881 | 24% |
Reaction Steps
To a solution of 3.75 g of 4-t-butylphenol in 40 ml of tetrahydrofuran was added 0.88 g of sodium hydride (oil dispersion). After stirring 30 minutes, 1 ml of hexamethylphosphoramide was added and a solution of 7.36 g of methyl α-bromo-α-[p-(p-nitrophenoxy)phenyl]acetate in 25 ml of tetrahydrofuran was added over a period of 30 minutes. The mixture was stirred at room temperature for 30 minutes and refluxed for 30 minutes. The mixture was poured into 130 ml of ice-water and extracted with dichloromethane. The extracts were washed with saturated sodium chloride solution and chilled. Filtration gave 2.1 g of product. The filtrate was concentrated to an oil under vacuum and chromatographed over silica gel (eluent-CCl4). From the first fractions there was obtained 4.3 g of solid which was dissolved in hot methanol and the volume reduced. Chilling gave 3.7 g of product as pale yellow crystals, mp 101° -103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125729 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-c74c737e2e324ee89c76e740cdfc9930 |
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| Source note | uspto-grants-1978_11 |
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