HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194771Generated: November 4, 2026
Ethyl 4-phenoxybenzoylformate → HCID 14329352, compound
https://huagongshe.com/reaction/1194771
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-phenoxybenzoylformate | HCID 2758881 | — |
| Reactant | HCID 15614287 | HCID 15614287 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14329352 | HCID 14329352 | 80% |
Reaction Steps
In 50 ml of anhydrous tetrahydrofuran was dissolved 1.58 g of 2-dimethylphosphoryl-1,3,5-trithiane, and 4 ml of 1.6M n-butyl lithium was added dropwise under an argon atmosphere at a temperature of about -70° C. After completion of the dropwise addition, the resulting mixture was stirred for 1 hour. Next, a solution of 1.41 g of ethyl 4-phenoxyphenylglyoxylate dissolved in 5 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to room temperature and the mixture thus obtained was stirred overnight. Thereafter, the same treatment as in Example 1 was carried out to give a crude product, which was then purified by a silica gel column chromatography (chloroform:hexane=2:1) to obtain 1.63 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816475 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-52a2312a28a14b619a528179bf8d7d12 |
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| Source note | uspto-grants-1989_03 |
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