HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(7-Chloroquinol-2-ylmethoxy)benzyl alcohol → 3-(6-Fluorobenzothiazol-2-ylmethoxy)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(7-Chloroquinol-2-ylmethoxy)benzyl alcohol | HCID 19737240 | — |
| Reactant | 3-(2-Pyridylmethoxy)benzyl alcohol | HCID 28561898 | — |
| Reactant | 3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl alcohol | HCID 53637583 | — |
| Reactant | 3-(5,6-Difluorobenzothiazol-2-ylmethyloxy)benzyl alcohol | HCID 53869797 | — |
| Product | 3-(6-Fluorobenzothiazol-2-ylmethoxy)benzyl alcohol | HCID 54235074 | — |
Reaction Steps
By a similar procedure 3-(5,6-difluorobenzothiazol-2-ylmethyloxy)benzyl alcohol, m.p. 98°-100° C., 3-(5-fluorobenzothiazol-2-ylmethoxy)benzyl alcohol, m.p. 139°-140° C., 3-(7-chloroquinol-2-ylmethoxy)benzyl alcohol, m.p. 128°-129° C., and 3-(2-pyridylmethoxy)benzyl alcohol, NMR (300 MHz, CDCl3) 5.10 (s, 2H) were prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322847 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-9a384f2a08cc44909985b9d7ab3c9c49 |
| Source note | uspto-grants-1994_06 |