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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969046Generated: November 3, 2026

Sodium borohydride → HCID 58288493, compound

https://huagongshe.com/reaction/1969046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58288510HCID 58288510—
SolventMethanolHCID 887—
ProductHCID 58288493HCID 58288493—

Reaction Steps

To [3-(2-formyl-4-trifluoromethyl-phenoxy)-phenyl]-acetic acid ethyl ester (0.411 g, 1.17 mmol) in MeOH (15 mL) was added sodium borohydride (0.045 g, 1.17 mmol), and the reaction was stirred for 15 minutes at room temperature. The mixture was concentrated, and the residue was partitioned between EtOAc and H2O. The aqueous layer was separated and extracted twice with EtOAc, and the combined organic layers were dried and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426449B2
Source datasetuspto-grants-2013_04
ORD IDord-6d93488edc8747aebb741768d0b4a9f8
Source noteuspto-grants-2013_04