HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639054Generated: October 25, 2026
4-Chloro-3-methylphenol → 4-Chloro-1-(4-chloro-3-methylphenoxy)-2-butanol
https://huagongshe.com/reaction/1639054
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3-methylphenol | HCID 1732 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dichloro-2-butanol | HCID 17021 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-1-(4-chloro-3-methylphenoxy)-2-butanol | HCID 13323908 | 22.3% |
Reaction Steps
To a mixture of 286 g (2 mole) of 3-methyl-4-chlorophenol, 700 ml of tertiary butanol, 700 ml of water and 3.0 mole of 1,4-dichloro-2-butanol, sodium hydroxide (2.9 moles, 230 g in 700 ml of water) was added with stirring at 40° C. to maintain a pH of 9.5-10.0 as the reaction progressed. The addition was 10 hr; the reaction was stirred at 40° C. for 48 hr. The resulting reaction mixture was extracted with chloroform sodium hydroxide at 25° C. The chloroform extract was washed with sodium sulfate. The dried chloroform solution was concentrated and the residue was distilled under reduced pressure to give 110.9 g of the product which distilled at 135°-143° C./0.007 mm and melted at 87°-89° C. after recrystallization with isopropanol and petroleum ether (30°-60° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04882330 |
|---|
| Source dataset | uspto-grants-1989_11 |
|---|
| ORD ID | ord-e6a02f8f2dde4a979e14dfca706495f2 |
|---|
| Source note | uspto-grants-1989_11 |
|---|