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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Iodo-N-methoxy-N-methyl-benzamide | HCID 5461756 | — |
| Reactant | 5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazole | HCID 12016670 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(3-Chlorophenyl)-2,1-benzisoxazol-5-yl](4-iodophenyl)-methanone | HCID 21082022 | 44% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173040B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-7d80e18f5eef4bf4b208f9fb9065299c |
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| Source note | uspto-grants-2007_02 |
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