HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106735Generated: October 25, 2026
Ethyl 4-formylbenzoate → Ethyl p-[2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]-benzoate
https://huagongshe.com/reaction/2106735
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-formylbenzoate | HCID 80498 | — |
| Reactant | [1-(4,5,6,7-Tetrahydro-4,4,7,7-tetramethylbenzo-[b]thien-2-yl)ethyl]triphenylphosphonium bromide | HCID 23049224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl p-[2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]-benzoate | HCID 53678243 | 55.5% |
Reaction Steps
30 g of [1-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)ethyl]triphenylphosphonium bromide and 9.5 g of 4-ethoxycarbonylbenzaldehyde are suspended in 300 ml of butylene oxide and the mixture is heated at reflux for 4 hours. The thus-obtained solution is concentrated to one third of the original volume in a water-jet vacuum, poured into 500 ml of a methanol/water mixture (6:4) and extracted several times with hexane. The organic phase is washed three times with water, dried over sodium sulphate and evaporated. There is obtained a light brownish oil which is purified by filtration over silica gel (eluting agent hexane/ether 19:1). After recrystallization from hexane, there are obtained 11.3 g of ethyl p-[2-(4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thien-2-yl)propenyl]benzoate in the form of colorless crystals, m.p. 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04931458 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-a8dcd1a8dc3e4851b7a8a71aa83d4d5e |
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| Source note | uspto-grants-1990_06 |
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