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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346973Generated: October 30, 2026

Water → [3-(3-Chlorophenyl)-2,1-benzisoxazol-5-yl](4-iodophenyl)-methanone

https://huagongshe.com/reaction/346973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Iodo-N-methoxy-N-methyl-benzamideHCID 5461756—
Reactant5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazoleHCID 12016670—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[3-(3-Chlorophenyl)-2,1-benzisoxazol-5-yl](4-iodophenyl)-methanoneHCID 2108202244%

Reaction Conditions

Temperature-70 °C

Reaction Steps

BuLi 1.6M (0.106 mol) was added dropwise at −70° C. to a solution of 5-bromo-3-(3-chlorophenyl)-2,1-benzisoxazole (0.0816 mol), obtained in Example A1a, in THF (250 ml) under N2 flow. The mixture was stirred at −70° C. for 15 min. A solution of 4-iodo-N-methoxy-N-methyl-benzamide (0.098 mol) in THF (150 ml) was added dropwise at −70° C. The mixture was stirred at −70° C. for 1 hour then brought to room temperature. The mixture was hydrolysed with water, extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue (48 g) was crystallized from diethyl ether. The precipitate was filtered off and dried, yielding 16.5 g (44%) of [3-(3-chlorophenyl)-2,1-benzisoxazol-5-yl](4-iodophenyl)-methanone, mp.196° C. (intermediate 35).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173040B2
Source datasetuspto-grants-2007_02
ORD IDord-7d80e18f5eef4bf4b208f9fb9065299c
Source noteuspto-grants-2007_02