HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416369Generated: October 25, 2026
1-(2,3-Dichlorophenyl)ethanol → 1-(2,3-Dichlorophenyl)ethan-1-one
https://huagongshe.com/reaction/1416369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2,3-Dichlorophenyl)ethanol | HCID 600228 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(2,3-Dichlorophenyl)ethan-1-one | HCID 91986 | 65% |
Reaction Steps
α-Methyl-2,3-dichlorobenzyl alcohol (5.0 g, 0.026 mol was dissolved in acetic acid (24 ml) and 12% w/v sodium hypochlorite solution (23.26 ml, 0.0314 mol) was added slowly dropwise, with stirring, at a temperature of 15-25° C. When the addition was complete the reaction mixture was stirred at ambient temperature for approximately 11/2 hours until a starch/iodide test gave a positive result. Saturated sodium bisulphite solution was added to the reaction mixture until the starch/iodide test was negative. The mixture was poured onto ice/brine (100 ml) and extracted with diethyl ether (3×75 ml). The ether phases were combined and washed with 2N sodium hydroxide solution (3×75 ml) until the aqueous washes were alkaline. The ether phase was dried over anhydrous magnesium sulphate, filtered and evaporated down. 2,3-Dichloroacetophenone (3.2 g, 65% yield) was afforded as a pale-yellow oil. T.l.c. (SiO2 ;CHCl3) and nmr showed this material to contain no impurities.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05912345 |
|---|
| Source dataset | uspto-grants-1999_06 |
|---|
| ORD ID | ord-937f85b3d7e34ef1a2c2897c62ae291c |
|---|
| Source note | uspto-grants-1999_06 |
|---|