HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333048Generated: October 30, 2026
Hydrochloric Acid → 1-Ethoxy-2,2,3,3,3-pentafluoro-1-Propanol
https://huagongshe.com/reaction/333048
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propanoic acid, 2,2,3,3,3-pentafluoro-, ethyl ester | HCID 67928 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Ethoxy-2,2,3,3,3-pentafluoro-1-Propanol | HCID 101655 | — |
Reaction Steps
Ethyl 2,2,3,3,3-pentafluoropropionate (10.99 grams, 57.2 mmol) was dissolved in anhydrous methanol (57 ml) and cooled under argon to −60° C. Sodium borohydride (2.16 grams, 57.2 mmol) was added in four portions. After the addition was complete, stirring was continued for one hour and the temperature was held below −45° C. The mixture was cooled to −60° C. and 1M hydrochloric acid (172 ml) was added dropwise so that the temperature remained below −45° C. The mixture was slowly warmed to room temperature and extracted with diethylether (3×100 ml). The combined organic phases were washed with water (two times), dried over magnesium sulfate, the solvent was removed under reduced pressure. 9.76 g (50.3 mmol, 88%) were obtained and used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877934B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-d958a42572334a8e86bf74fd219a55db |
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| Source note | uspto-grants-2014_11 |
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