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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542903Generated: October 27, 2026

Methanol--water (1/1) → Ethyl 3-methyl-7-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)-2,4,6-octatrienoate

https://huagongshe.com/reaction/542903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanol--water (1/1)HCID 22242641—
Reactant[1-(4,5,6,7-Tetrahydro-4,4,7,7-tetramethylbenzo-[b]thien-2-yl)ethyl]triphenylphosphonium bromideHCID 23049224—
ReactantEthyl 5-formyl-3-methyl-2,4-pentadienoateHCID 54439227—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-methyl-7-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)-2,4,6-octatrienoateHCID 5388283583.3%

Reaction Steps

4.50 g of [1-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)ethyl]triphenylphosphonium bromide and 1.3 g of ethyl 5-formyl-3-methylpenta-2,4-dienoate are dissolved in 70 ml of butylene oxide and the solution is heated at reflux for 2 hours. The cooled mixture is poured into a methanol/water mixture (6:4) and extracted several times with hexane. The hexane phase is washed three times with water, dried and evaporated. After filtration of the crude product over silica gel (eluting agent hexane/ether 9:1), there are obtained 2.4 g of ethyl 3-methyl-7-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)-2,4,6,-octatrienoate as a pale yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659735
Source datasetuspto-grants-1987_04
ORD IDord-3a698e2121af45f3a1fb5a518e8e9a07
Source noteuspto-grants-1987_04