HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036448Generated: October 31, 2026
N-Iodosuccinimide → HCID 178445720, compound
https://huagongshe.com/reaction/1036448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 178445718 | HCID 178445718 | — |
| Catalyst | Zirconium chloride (ZrCl4), (T-4)- | HCID 9856075 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178445720 | HCID 178445720 | 79.2% |
Reaction Steps
To a solution of 2-Bromo-6-(trans-4-tert-butyl-cyclohexyloxy)-naphthalene (500 mg, 0.001 mol) in Methylene chloride (2 mL, 0.03 mol), N-iodosuccinimide (600 mg, 0.003 mol) was added, followed by zirconium tetrachloride (60 mg, 0.0003 mol) at 23° C. The reaction mixture was then sonicated and stirred for 5 minutes at 23° C. Reaction was then diluted with DCM and the solids were removed via filtration through a 4 micron filter. 1 g of SiO2 was added directly to the solution and the solvent was then removed under reduced pressure. The SiO2 was then loaded onto a column (SiO2, 24 g, 0-10% ethyl acetate/hexanes (ran neat hexanes for first 9 minutes of a 30 min gradient)) to give the DP as a tan amorphous solid with 20% impurity (SM) by HNMR. Material was then triturated with methanol, filtered, and dried on filter to give 386 mg of the desired product as a white solid in (60%). ESI-MS: 488 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546359B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-391ef005d9e242d5882e890f400ce38e |
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| Source note | uspto-grants-2013_10 |
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