HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461776Generated: November 1, 2026
Dimethyl Sulfoxide → Ethyl [(5-oxopentyl)oxy]acetate
https://huagongshe.com/reaction/1461776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Ethyl [(5-hydroxypentyl)oxy]acetate | HCID 14254559 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl [(5-oxopentyl)oxy]acetate | HCID 14254560 | 84% |
Reaction Steps
To a solution of dimethylsulphoxide (18.6 ml, 263 mmol) in 75 ml of CH2Cl2 at -60° C. under nitrogen, is added dropwise a solution of trifluoroacetic anhydride (27.8 ml, 197 mmol) in 75 ml of CH2Cl2, over about 15 minutes. The reaction mixture is stirred for a further 15 minutes at -60° C. and the hydroxy/ester (1) (25 g, 132 mmol) in 150 ml CH2Cl2 is then added at such a rate as to keep the reaction temperature below -60° C. (over about 30 minutes). After a further 15 minutes at this temperature, triethylamine (55 ml, 395 mmol) is added slowly over about 15 minutes, the reaction mixture is allowed to warm to ambient temperature (about 1.5 hours) and is then quenched with water. The product is isolated by extraction with dichloromethane and purified by chromatography on Florisil to provide the title compound as an oil (20.7 g, 84%), νmax (film) 1750, 1725, 1195, 1130 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05077309 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-7184ede34e404a8893fd7629ac1af93c |
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| Source note | uspto-grants-1991_12 |
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