HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59712Generated: October 30, 2026
Trifluoromethanesulfonyl chloride → HCID 55256123, compound
https://huagongshe.com/reaction/59712
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonyl chloride | HCID 79000 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Amino-3-(pyridin-3-yl)propanoic acid | HCID 3606547 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 55256123 | HCID 55256123 | 42% |
Reaction Steps
To a mixture of 20.20 g (0.24 mole) sodium bicarbonate (Sigma, Ultrapure, dried in good vacuum at room temperature for 3 days over phosphorus pentoxide) and 6.64 g (0.04 mole) 3-amino-3-(pyridine-3-yl)propionic acid (Tyger, dried in good vacuum at room temperature for 3 days over phosphorus pentoxide) under argon atmosphere first 200 ml of dry acetonitrile (Fisher) was added then at very strong stirring 4.7 ml (0.044 mole) trifluormethanesulfonyl chloride (Acros) was slowly added and thereafter the reaction mixture was further stirred in an oil bath of 75-80° C. for 19 hours. After cooling and stirring in ice bath for 1 hour the reaction mixture was filtered, washed three times with dry acetonitrile and the combined organic solutions were evaporated on a rotavapor at 35° C. The solid residue (23.8 g) was extracted in a Soxhlet-type extractor with boiling chloroform for 26 hours. The evaporation of the chloroform solution gave 2.48 g (42%) pure product as white crystalline material (mp: 115-116° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440948B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-bbf56ee647a448dbb5b19014e52ea0bb |
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| Source note | uspto-grants-2016_09 |
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