HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → 3-[3-(1-Pyrrolyl)benzylthio]benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | 3-Sulfanylbenzaldehyde | HCID 14946834 | — |
| Reactant | 3-(1-Pyrrolyl)benzyl methanesulfonate | HCID 19744531 | — |
| Product | 3-[3-(1-Pyrrolyl)benzylthio]benzyl alcohol | HCID 54259385 | — |
Reaction Steps
3-[3-(3-thienyl)benzyloxy]benzyl alcohol, 3-[4-(3-thienyl)-2-thienylmethylthio]benzyl alcohol, 3-[3-(5-oxazolyl)benzylthio]benzyl alcohol, 3-[3-(5-oxazolyl)benzylthio]benzyl alcohol and 3-[3-(1-pyrrolyl) benzyloxy]benzyl alcohol are obtained by performing the same reaction as in Referential Example 57 except that instead of the starting 3-(1-pyrrolyl)benzyl methanesulfonate and/or 3-mercaptobenzaldehyde, the corresponding methanesulfonate and/or 3-hydroxybenzaldehyde are used.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234946 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-61f9634e9b2c4e339a2637f55c4cd35f |
| Source note | uspto-grants-1993_08 |