HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 54351123, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tris(2-chloroethyl) phosphite | HCID 8783 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 54351123 | HCID 54351123 | — |
Reaction Steps
The same equipment and procedure as in Example 1 was employed. The reaction flask was charged with 100 ml ethylene dichloride and 85 g acetyl chloride (1.1 mole). The addition of 270 g (1.0 mole) tris (β-chloroethyl) phosphite was commenced dropwise and continued for one hour during which there was a slow exotherm to 35° C. After addition of the triphosphite the reaction continued with a self-maintained exotherm at about 40° C. for three hours and then a slow return to ambient temperature while stirring overnight. The pink acetyl bis(β-chloroethyl) phosphite was isolated by rotary evaporatory at 50° C. and 15 torr. The yield was 261 g; acid number 2; purity by infrared analysis was about 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04407765 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-7f2eae64cf9d43a7a79072298464b4a8 |
| Source note | uspto-grants-1983_10 |