Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-Chloro-2-propanol | HCID 31370 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13053832 | HCID 13053832 | — |
Reaction Steps
94.5g (1 mol) of chloroacetic acid and 154.7g of potassium bromide were put into a 1 liter four necked flask equipped with a stirrer, a thermometer, a reflux condenser and a dropping funnel. To the mixture were added 100 ml of water as a reaction medium and stirred vigorously. Then 127.4g (1.3 mol) of c.-- sulfuric acid were added droppwise over the course of an hour at a constant rate. During that time, the temperature of the reaction mixture rose to about 50° C. After the droppwise addition, stirring was continued for an hour at 55° C. Then 94.5g (1 mol) of 1-chloro-2-propanol and 200g of toluene were added to the reaction mixture, and refluxed for an hour at 100° ~ 110° C in an oil bath. A receiver was attached to a reflux condenser and water was removed from the reaction mixture by azeotropic distillation with toluene. Then the resultant crystals of potassium hydrogen sulfate were filtered off from the reaction mixture to give a toluene solution of 1-chloro-2-propyl bromoacetate, which was sufficient to use industrially as it is. But if needed, toluene was removed from the filtrate followed by distillating the residue to give 201.2g (93.4% of theory) of 1-chloro-2-propyl bromoacetate of bp 76° ~ 77° C (2 mmHg) as a colorless and clear liquid. nD25 = 1.4780, D420 = 1.5933. 176.6g (99.8%) of potassium hydrogen sulfate was isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04123443 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-dfc122d174c34adb836390868c783ddf |
|---|
| Source note | uspto-grants-1978_10 |
|---|