HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623501Generated: October 31, 2026
2,2,3,3,3-Pentafluoropropanol → HCID 87426740, compound
https://huagongshe.com/reaction/623501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,3,3,3-Pentafluoropropanol | HCID 9872 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 87426740 | HCID 87426740 | 71.8% |
Reaction Steps
To a stirred suspension of sodium hydride (4.9 g, 120 mmol, 60% in oil) in N,N-dimethylacetamide (100 mL) is added dropwise 2,2,3,3,3-pentafluoropropan-1-ol (8.1 mL, 82 mmol) at 0° C. After stirring for 10 minutes, a solution of methyl 6-chloronicotinate (7.0 g, 41 mmol) in N,N-dimethylacetamide (120 mL) is added dropwise at 0° C., and the mixture is stirred for 30 minutes at room temperature. Then, the mixture is stirred at 90° C. for 2 hours. After cooled to room temperature, 2M aqueous sodium hydroxide is added (pH is around 6). The mixture is extracted with n-hexane/ethyl acetate (1:2, 200 mL). The organic layer is washed with water, brine, and dried over sodium sulfate. The organic solvent is concentrated under reduced pressure to give 8.4 g of the title compound as a crude product (include 2,2,3,3,3-pentafluoropropyl 6-(2,2,3,3,3-pentafluoropropoxy)nicotinate as a byproduct). The residue is used for the next reaction (Step-2) without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09302991B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-b9f5a949e7f5462eae306efa5f86caf3 |
|---|
| Source note | uspto-grants-2016_04 |
|---|