HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [2-(2-Thienyl)-1,3-thiazol-4-YL]methanol | HCID 2776319 | — |
| Product | 4-(Chloromethyl)-2-(thiophen-2-yl)-1,3-thiazole | HCID 736496 | 65% |
Reaction Steps
In substantially the same manner as in Reference Example 73, 2-(2-thienyl)-4-thiazolylmethanol was allowed to react with thionylchloride to give 4-chloromethyl-2-(2-thienyl)thiazole. The yield was 65%. Recrystallization from ethyl acetate-hexane gave colorless needles, mp 54-55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211215B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-5a7fb9cf4746443198935858846d7d80 |
| Source note | uspto-grants-2001_04 |