HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086065Generated: October 31, 2026
Tert-butyl acetoacetate → 1,1-Dimethylethyl 9,9-bis(4-fluorophenyl)-5-hydroxy-8-(1-methylethyl)-3-oxo-6,8-nonadienoate
https://huagongshe.com/reaction/1086065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5,5-Bis(4-fluorophenyl)-4-(1-methylethyl)-2,4-pentadienal | HCID 53873949 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1-Dimethylethyl 9,9-bis(4-fluorophenyl)-5-hydroxy-8-(1-methylethyl)-3-oxo-6,8-nonadienoate | HCID 53726151 | 66.4% |
Reaction Steps
To a solution of 5,5-bis(4-fluorophenyl)-4-(1-methyl-ethyl)-2,4-pentadienal (0.5 g, 1.6 mmol) in 20 mL tetrahydrafuran at -70° C., was added the dianion of t-butyl acetoacetate (2.1 mL of 1M solution in THF, 2.1 mmol) which was prepared by adding t-butyl acetoacetate (4.0 g, 25 mmol) in 4 mL tetrahydrofuran to a suspension of sodium hydride (1.0 g of 50% in oil, 25 mmol) in 6 mL tetrahydrofuran at -10° C., butyl lithium (11.4 mL of 2.2M solution) 25 mL was added and stirred for 0.5 hrs. After stirring for 2.5 hrs. the reaction was quenched with 2N hydrochloric acid. The mixture was extracted with diethyl ether. The extracts were dried over magnesium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel eluting with 1% methanol in methylene chloride to give 0.5 g of the title compound as a clear oil. MS(CI): m/e =370 for M3 ;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05011947 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-facfd26347cf4bd6b0607a1209ee49e2 |
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| Source note | uspto-grants-1991_04 |
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