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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456819Generated: October 30, 2026

methyl 2-{[6-(1-benzyl-5-phenyl-1H-pyrrol-2-yl)-2-naphthyl]oxy}-3-phenylpropanoate → 2-{[6-(1-Benzyl-5-phenyl-1H-pyrrol-2-yl)-2-naphthyl]oxy}-3-phenylpropanoic acid

https://huagongshe.com/reaction/456819

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 2-{[6-(1-benzyl-5-phenyl-1H-pyrrol-2-yl)-2-naphthyl]oxy}-3-phenylpropanoateHCID 18439043—
SolventWaterHCID 962—
Product2-{[6-(1-Benzyl-5-phenyl-1H-pyrrol-2-yl)-2-naphthyl]oxy}-3-phenylpropanoic acidHCID 1165658490%

Reaction Steps

In a similar manner as described in step 7 of Example 1, the title compound was prepared from methyl 2-{[6-(1-benzyl-5-phenyl-1H-pyrrol-2-yl)-2-naphthyl]oxy}-3-phenylpropanoate (0.145 g, 0.270 mmol), prepared in the previous step, and the addition of water (3 mL) to the reaction mixture. After the volatiles were removed under reduced pressure, the residue was partitioned between water and methylene chloride. The layers were separated and the aqueous layer was extracted one time with methylene chloride. The combined extracts were dried (MgSO4), filtered and the solvent removed under reduced pressure to give the title compound as an off-white solid (0.127 g, 90%), mp 70–80° C. Elemental Analysis for C36H29NO3.0.48 H2O Calc'd: C, 81.23; H, 5.67; N, 2.63. Found: C, 80.67; H 6.28; N, 2.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186749B2
Source datasetuspto-grants-2007_03
ORD IDord-fba7a89705f547f58e8ee32c2cf0590b
Source noteuspto-grants-2007_03