HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzyl alcohol → Benzenemethanol, 3-(2-quinolinylmethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzyl alcohol | HCID 102 | — |
| Reactant | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| Reactant | 2-(Chloromethyl)quinoline | HCID 20394 | — |
| Product | Benzenemethanol, 3-(2-quinolinylmethoxy)- | HCID 14650410 | 85% |
Reaction Steps
The procedure from Example 6, part A was used except 2-(chloromethyl)quinoline was substituted for 7chloro-(2-chloromethyl)quinoline and 3-hydroxybenzyl alcohol was substituted for 4-hydroxybenzyl alcohol. The intermediate was obtained in 85% yield: mp 82°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622969 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-dd758f7908b94354828ffdecb5b6978d |
| Source note | uspto-grants-1997_04 |