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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427742Generated: November 3, 2026

Tert-butyl 1-((4-(4-(3-aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate → 1-((4-(4-(3-Aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oic acid

https://huagongshe.com/reaction/1427742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 1-((4-(4-(3-aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oateHCID 90411873—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product1-((4-(4-(3-Aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oic acidHCID 90412331109.6%

Reaction Steps

tert-butyl 1-((4-(4-(3-aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate (3.24 g, 5.63 mmol) was dissolved in a solution of DCM:TFA (2:1, 20 ml) and stirred ca. 1 h. Upon completion, reaction was then concentrated under reduced pressure, co-evaporated with toluene, and dried on oil pump for 5 hs to yield 3.20 g of crude 1-((4-(4-(3-aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oic acid as yellow oil. The crude product was used without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933261B2
Source datasetuspto-grants-2015_01
ORD IDord-f9f76e322ed0462c92d05029c5325c2c
Source noteuspto-grants-2015_01