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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263134Generated: October 25, 2026

Water → 5-[2,6,6-trimethyl-3-oxo-4(S)-(phenoxyacetoxy)-cyclohex-1-en-1-yl]-3-methyl-penta-2,4-dien-1-al

https://huagongshe.com/reaction/263134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantPhenoxyacetyl chlorideHCID 69703—
ReactantRac. 5-(2,6,6-trimethyl-3-oxo-4-hydroxy-cyclohex-1-en-1-yl)-3-methyl-penta-2,4-dien-1-alHCID 73769876—
SolventDiethyl EtherHCID 3283—
Product5-[2,6,6-trimethyl-3-oxo-4(S)-(phenoxyacetoxy)-cyclohex-1-en-1-yl]-3-methyl-penta-2,4-dien-1-alHCID 53795135—

Reaction Conditions

Temperature0 °C

Reaction Steps

14 g of the hydroxyketoaldehyde of formula XIII obtained in Example 26 are dissolved in 200 ml of diethyl ether. 20 ml of pyridine are added to the solution at 0° C. and 12 g of phenoxyacetic acid chloride are then added dropwise. The mixture is stirred for 2 hours at 0° C. and then poured into water and extracted with diethyl ether. The 5-[2,6,6-trimethyl-3-oxo-4(S)-(phenoxyacetoxy)-cyclohex-1-en-1-yl]-3-methyl-penta-2,4-dien-1-al (IIA) is isolated from the ether extract.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04156090
Source datasetuspto-grants-1979_05
ORD IDord-afd8878daa1a4d32ae01c955d8fed9e6
Source noteuspto-grants-1979_05