HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020890Generated: November 1, 2026
Trifluoromethanesulfonic anhydride → HCID 10517725, compound
https://huagongshe.com/reaction/1020890
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Ethyl 6-hydroxyhexanoate | HCID 357781 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10517725 | HCID 10517725 | 75% |
Reaction Steps
To the suspension of poly(4-methylpyridine) (2.24 g, 2 eq) in newly dried dichloromethane (25 mL ) at 0° C. was added trifluoromethanesulfonic anhydride (5 g, 1 eq) drop wise over 30 mins. Ethyl 6-hydroxyhexanoate (2.76 g, 0.95 eq) was then added in drop wise via a syringe. The mixture was stirred at 0° C. for 4 hrs and the polymer was filtered off by a frit. The solvent was evaporated under reduced pressure (without heating) and the crude product was subjected to a short silica gel pad with 1:4 (v/v) diethyl ether/hexane as the eluent solvent. The solvent was evaporated (without heating) and the product was used directly in the following step. (3.9 g, 75% yield based on ethyl 6-hydroxyhexanoate.) See FIG. 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716491B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-1decd84120c040069954e7c809639666 |
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| Source note | uspto-grants-2014_05 |
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