HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-1-fluoro-4-nitrobenzene → 3-Chloro-4-(2-thiazolylthio)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-1-fluoro-4-nitrobenzene | HCID 67688 | — |
| Reactant | HCID 178527881 | HCID 178527881 | — |
| Product | 3-Chloro-4-(2-thiazolylthio)nitrobenzene | HCID 18967602 | 26% |
Reaction Steps
Using an analogous procedure to that described in the first paragraph of the portion of Example 8 which is concerned with the preparation of starting materials, 3-chloro-4-fluoronitrobenzene was reacted with 2-thiazolethiol to give a precipitated solid which was partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated to give 2-chloro-4-nitrophenyl 2-thiazolyl sulphide in 26% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05821246 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-ef581cff486446fe8604b1eb80db8312 |
| Source note | uspto-grants-1998_10 |