HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525971Generated: November 1, 2026
Trifluoroacetic acid → HCID 59193269, compound
https://huagongshe.com/reaction/1525971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 86639147 | HCID 86639147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59193269 | HCID 59193269 | 98% |
Reaction Steps
To a solution of tert-butyl 2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidopropylcarbamate (2.10 g, 4.34 mmol) in DCM (100 mL) at 0° C. was slowly added TFA (30 mL). The mixture was stirred (0° C., 2 h), warmed to RT and stirred (16 h). The mixture was basified to pH 10 with saturated aqueous Na2CO3 and extracted with EtOAc (2×200 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure to afford (4Z,7Z,10Z,13Z,16Z,19Z)—N-(1-aminopropan-2-yl)-docosa-4,7,10,13,16,19-hexaenamide (1.60 g, 98%) as a light yellow oil. Mass calculated for C25H40N2O=384.6; found: [M+H]+=385.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085527B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-71eb0919e3284f51892d4dd3f6e379dd |
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| Source note | uspto-grants-2015_07 |
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