HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Cyclopentyloxy-4-methoxybenzaldehyde → HCID 10225770, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Cyclopentyloxy-4-methoxybenzaldehyde | HCID 2735893 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 22618269 | HCID 22618269 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10225770 | HCID 10225770 | 59.8% |
Reaction Steps
By employing a procedure similar to that in Example 33 and using 2-(3-chlorophenyl)-7-aminobenzoxazole (1.00 g, 0.0041 mol), 3-cyclopentyloxy-4-methoxybenzaldehyde (1.08 g, 0.0049 mol), sodium cyanoborohydride (0.41 g, 0.0065 mol) and 35 ml of methanol, a white, crystalline solid was isolated. This crude product (1.4 g) was recrystallized from 200 ml of methanol to yield the title compound (1.1 g), mp 133-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372770B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-37b65a7f32674b4eb262e75e04ba0287 |
| Source note | uspto-grants-2002_04 |