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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639210Generated: November 1, 2026

Salicylaldehyde → HCID 14676386, compound

https://huagongshe.com/reaction/1639210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantHCID 14676385HCID 14676385—
ProductHCID 14676386HCID 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-[(2,2dimethyl-octyl]phenyl]-2,4,5,8-non-atetraenoic acid mp 113-117° (from dichloromethane/hexane mixture).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04883614
Source datasetuspto-grants-1989_11
ORD IDord-1fb0347b741848aa94bd4771fc3a216f
Source noteuspto-grants-1989_11