HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654274Generated: November 2, 2026
2,2,2-Trifluoroethanol → 2,2,2-Trifluoroethyl trifluoroacetate
https://huagongshe.com/reaction/1654274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Trifluoroacetyl chloride | HCID 61106 | — |
| Reactant | pyridine TFA | HCID 9813011 | — |
| Product | 2,2,2-Trifluoroethyl trifluoroacetate | HCID 67888 | 566.8% |
Reaction Steps
30 g (0.16 mole) of pyridinium trifluoroacetate in 355 g (3.55 mole) of 2,2,2-trifluoroethanol were introduced as an initial charge into a laboratory circulating reactor apparatus (one-liter four-necked flask fitted with KPG stirrer, a Prominent pump, and a 30 cm column packed with Raschig rings), and the initial charge was circulated at an internal temperature of 54° C. 134 g (1.01 mole) of trifluoroacetyl chloride were subsequently metered into the flask via an immersed inlet tube over a period of 100 minutes. After the trifluoroacetyl chloride addition was complete, the mixture was allowed to react for a further 10 minutes. Subsequent fractional distillation of the reaction mixture via a Vigreux column (temperature at the distillation head: from 54° to 56° C.) yielded 177.8 g of trifluoroethyl trifluoroacetate, corresponding to 89.8% of the theoretical yield. The trifluoroethanol/pyridinium salt mixture remaining in the reservoir flask can be used again for esterification with equal effectiveness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05405991 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-be7ab524c7a74ff49ecf07a8293dd2e0 |
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| Source note | uspto-grants-1995_04 |
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