HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylaldehyde → HCID 14676386, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | HCID 14676385 | HCID 14676385 | — |
| Product | HCID 14676386 | HCID 14676386 | — |
Reaction Steps
2-Hydroxybenzaldehyde was condensed with 2,2-dimethyl-1-iodo octane to yield 2-(2,2-dimethyl octyloxy) benzaldehyde which was reduced to 2-(2,2-dimethyl octyloxy)benzyl alcohol and then converted to [2-(2,2-dimethyloctyloxy)phenyl]methyl]triphenylphosphonium bromide as in Example 1. Condensation of this phosphonium bromide with 7-formyl-3-methyl-2,4,6-octatrienoic acid ethyl ester as described in Example 3 followed by hydrolysis, as in Example 5, gave the (All-E)-3,7-Dimethyl-9-[2-[(2,2- dimethyl-octyl)oxy]phenyl]-2,4,5,8-non-atetraenoic acid mp 113°-117° (from dichloromethane/hexane mixture).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04894480 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-d09efeadfaac49bdaddf7a9665ae1ac3 |
| Source note | uspto-grants-1990_01 |