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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056128Generated: November 1, 2026

Trifluoroacetic acid → HCID 131736418, compound

https://huagongshe.com/reaction/1056128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89785008HCID 89785008—
SolventDichloromethaneHCID 6344—
ProductHCID 131736418HCID 131736418—

Reaction Conditions

Temperature40 °C

Reaction Steps

An orange solution of (R)-tert-butyl 2-(3-(benzyloxy)-1-((tert-butoxycarbonyl)amino)propyl)-1-tosyl-1H-pyrrole-3-carboxylate (504c, 5.85 g, 10.00 mmol) in DCM (15 mL) was treated with TFA (15 mL, 202 mmol) and heated at 40° C. for 2 h. The TFA and DCM was removed in vacuo affording (R)-2-(1-amino-3-(benzyloxy)propyl)-1-tosyl-1H-pyrrole-3-carboxylic acid compound with 2,2,2-trifluoroacetic acid (1:1) (724d) as a dark orange viscous oil which was used for the next step without purification. m/z (ESI, +ve) 429.2 (M+1)′.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-70ef5c521609405eb369373c3a0c734c
Source noteuspto-grants-2016_07