HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → HCID 20027606, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-[(2-Methoxyphenoxy)methyl]-1,3-thiazolidine | HCID 3025454 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 20027606 | HCID 20027606 | 87% |
Reaction Steps
A solution of 2-(o-methoxyphenoxymethyl)thiazolidine (15 g) in acetone (75 ml), cooled at 10° C., under stirring is added with triethylamine (10.5 ml) and dropwise with a solution of α-chloroacetylchloride (5.8 ml) in acetone (15 ml). After 2 hours the mixture is added with potassium thioacetate (35.4 g) and stirring is continued for 2 hours, the mixture is poured in ice and water (250 ml) and the precipitate is filtered and crystallized from EtOH to give 2-(o-methoxyphenoxy)methyl-3-acetylthioacetylthiazolidine (19.8 g, 87% yield) m.p. 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04798898 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-0632a7352f294cd7a2761b928975eb82 |
| Source note | uspto-grants-1989_01 |