HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Hydroxyphenyl)benzothiazole → HCID 20284645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Hydroxyphenyl)benzothiazole | HCID 95745 | — |
| Reactant | HCID 19747006 | HCID 19747006 | — |
| Product | HCID 20284645 | HCID 20284645 | — |
Reaction Steps
A hot solution of 16 g. of zinc, o-aminophenylmercaptide and 12.5 g. of p-hydroxybenzaldehyde in 1 l. of acetic acid was treated with hydrogen sulfide for two hours, filtered hot, diluted with an equal volume of water and cooled. 2-(p-Hydroxyphenyl)benzothiazole (47% yield, m.p. 227°-229° F.) was obtained. The 2-(p-hydroxyphenyl)benzothiazole was reacted with 4-(2-bromoethoxy)-2-hydroxybenzophenone as in Example 1 to produce 4-(2-[4-(2-benzothiazolyl)phenoxy]ethoxy)-2-hydroxybenzophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256626 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-0e65f1be791b4c298741a5f1cc2c9cb8 |
| Source note | uspto-grants-1981_03 |