HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650390Generated: October 25, 2026
Acetyl chloride → 1-(4'-t-Butyldimethylsilyloxy-3'-methoxyphenyl)-1-hexene-3,5-dione
https://huagongshe.com/reaction/1650390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Reactant | 1-(4'-t-Butyldimethylsilyloxy-3'-methoxyphenyl)-1-butene-3-one | HCID 54529210 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4'-t-Butyldimethylsilyloxy-3'-methoxyphenyl)-1-hexene-3,5-dione | HCID 54156483 | 34.3% |
Reaction Steps
A solution of 1-(4'-t-butyldimethylsilyloxy-3'-methoxyphenyl)-1-butene-3-one (12.8 g, 41.8 mmol) in THF (50 mL) is cooled to -78° C. under an argon atmosphere. Lithium di-isopropyl amide (83.5 mmol, in 50 mL THF) is slowly added to the reaction mixture. The reaction is stirred at -78° C. for 30 minutes. Acetyl chloride (16.4 g, 209 mmol) dissolved in THF (20 mL) is then added to the reaction over a 30 minute period. The reaction is quenched with aqueous HCl. The layers are separated, and the aqueous layer is washed with ethyl acetate. The combined organic layers are washed with saturated aqueous sodium bicarbonate, dried over MgSO4, and evaporated to give a red oil. Flash chromatography (ethyl ether/hexane 2:8) afford 5.0 g (34%) of 1-(4'-t-butyldimethylsilyloxy-3'-methoxyphenyl)-1-hexene-3,5-dione, mp=81°-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04924002 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-bd9c0fd87dc9417d9668c4d6379a675e |
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| Source note | uspto-grants-1990_05 |
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