HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → HCID 19756597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | HCID 10753946 | HCID 10753946 | — |
| Reactant | HCID 178459950 | HCID 178459950 | — |
| Product | HCID 19756597 | HCID 19756597 | — |
Reaction Steps
The appropriate alcohol starting material was obtained as follows: 3(Naphth-2-ylmethoxy)benzaldehyde [prepared by the alkylation of 3-hydroxybenzaldehyde with 2-bromomethylnaphthalene in the presence of potassium carbonate] was treated with isopropoxydimethysilylmethylmagnesium chloride using the procedure described in the portion of Example 1 which is concerned with the preparation of starting materials. After the oxidation step described therein there was obtained 2-[3-(naphth-2-ylmethoxy)phenyl]ethane-1,2-diol, m.p. 121°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05214069 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-3af684738f2143218e35c1ca90af8e2d |
| Source note | uspto-grants-1993_05 |