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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056403Generated: October 31, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/1056403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89793961HCID 89793961—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 89793960HCID 89793960—
ProductHCID 131736425HCID 131736425—

Reaction Conditions

Temperature40 °C

Reaction Steps

An orange solution of (R)-tert-butyl 2-(1-((tert-butoxycarbonyl)amino)propyl)-1-tosyl-1H-pyrrole-3-carboxylate (505c, 6.19 g, 12.93 mmol) in DCM (15 mL) was treated with TFA (15 mL, 202 mmol) and heated at 40° C. for 4 h. The TFA and DCM was removed in vacuo affording (R)-2-(1-aminopropyl)-1-tosyl-1H-pyrrole-3-carboxylic acid compound with TFA (1:1) as a viscous orange oil (505d) which was used the next step without further purification. m/z (ESI, +ve) 323.1 (M+1)′.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-227ac907f8a54d81a0b2126778b4a496
Source noteuspto-grants-2016_07