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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372632Generated: October 31, 2026

Tetrahydrofuran → 3-Chloro-4-(1-indolinylcarbonylamino)phenylacetic acid

https://huagongshe.com/reaction/1372632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetateHCID 17859294—
SolventHydrochloric AcidHCID 313—
Product3-Chloro-4-(1-indolinylcarbonylamino)phenylacetic acidHCID 1785886360.4%

Reaction Steps

To ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate (3.07 g, 8.56 mmol) were added 0.25N NaOH (68.4 ml, 17.1 mmol) and THF (70 ml). The mixture was heated and refluxed for 4 hours. After cooling, the reaction mixture was poured in 1N hydrochloric acid (50 ml). The crystals thus precipitated were collected by filtration, and dried under reduced pressure for 12 hours, whereby 3-chloro-4-(1-indolinylcarbonylamino)phenylacetic acid (1.71 g, 60%) was obtained as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-bc9fae70bf514bc6a664cab11690dfa2
Source noteuspto-grants-2007_01