HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromodiphenylmethane → [(2-Diphenylmethylthio-4,5-dihydronaphtho[1,2-d]thiazol-8-yl)oxy]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | HCID 178472936 | HCID 178472936 | — |
| Product | [(2-Diphenylmethylthio-4,5-dihydronaphtho[1,2-d]thiazol-8-yl)oxy]acetic acid | HCID 18471107 | 90% |
Reaction Steps
Using ethyl [(2-mercapto-4,5-dihydronaphtho[1,2-d]thiazol-8-yl)oxy]acetate and bromodiphenylmethane, the procedure of Example 1 was otherwise repeated to synthesize the title compound. Yield 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06417213B2 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-463cb6addc0c44ab9fbb8781bab9bfa8 |
| Source note | uspto-grants-2002_07 |