HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459683Generated: October 29, 2026
Ethyl bromoacetate → [(7,7,8,8,8-Pentafluorooctyl)oxy]Acetic Acid
https://huagongshe.com/reaction/459683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7,7,8,8,8-Pentafluorooctan-1-ol | HCID 2775949 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(7,7,8,8,8-Pentafluorooctyl)oxy]Acetic Acid | HCID 9835343 | 39.6% |
Reaction Steps
To a stirred solution of 6-(pentafluoroethyl)hexan-1-ol (500 mg) in tetrahydrofuran (10 ml) was added sodium hydride (60% dispersion in mineral oil; 118 mg) and the reaction was stirred at 20° C. for 30 mlnutes. Ethyl bromoacetate (379 mg) was added and the reaction was stirred for a further 3 hours. The reaction was quenched by the addition of ethanol (3 ml) followed by stirring for 30 mlnutes, then 2M sodium hydroxide (3 ml) was added and the reaction was stirred for a further 2 hours. The reaction mixture was partitioned between dichloromethane (100 ml) and water (100 ml). The aqueous layer was acidified to pH 1 by the addition of 2M hydrochloric acid and then extracted with dichloromethane (3×100 ml). The combined organic layers were dried over magnesium sulphate and the solvent was removed in vacuo to give the title compound as a white solid (250 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07195752B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-d707a3df10714dff82ef28cebb2bcaf3 |
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| Source note | uspto-grants-2007_03 |
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