HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940253Generated: October 30, 2026
Tert-Butyl hypochlorite → 4-(1-(4-Isopropyloxyphenyl)-1-methylethyl)-2-chlorophenol
https://huagongshe.com/reaction/1940253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | 4-(1-(4-Isopropyloxyphenyl)-1-methylethyl)phenol | HCID 21466220 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(1-(4-Isopropyloxyphenyl)-1-methylethyl)-2-chlorophenol | HCID 21466367 | 85.2% |
Reaction Steps
To a solution of 4-(1-(4-isopropyloxyphenyl)-1-methylethyl)phenol (0.51 g) in carbon tetrachloriode (1.3 ml), a solution prepared by dissolving 0.23 g of tert-butyl hypochlorite in 0.5 ml of carbon tetrachloride was added dropwise with stirring under ice cooling. After 30 minutes, an ice bath was removed, and the mixture was stirred at room temperature for 30 minutes. The reaction solution was poured into water and extracted three times with 5 ml of carbon tetrachloride. Then, the carbon tetrachloride layers were combined, washed with water, dried over anhydrous magnesium sulfate and then concentrated to give a crude product. This crude product was subjected to silica gel column chromatography to give 0.49 g of 4-(1-(4-isopropyloxyphenyl)-1-methylethyl)-2-chlorophenol (yield, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698702 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-1613a11ece264029b3f458529d2ba9cd |
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| Source note | uspto-grants-1997_12 |
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