HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231433Generated: October 31, 2026
Carbon tetrabromide → HCID 20032357, compound
https://huagongshe.com/reaction/231433
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-[4-Chloro-2-fluoro-5-(hydroxymethyl)phenyl]-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione | HCID 13629754 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20032357 | HCID 20032357 | — |
Reaction Steps
To a stirred solution of 3.0 g (0.0097 mole) of of N-(4-chloro-2-fluoro-5-hydroxymethylphenyl)-3,4,5,6-tetrahydrophthalimide, prepared by the method of Example 4, and 6.4 g (0.0194 mole) of carbon tetrabromide in 30 ml of diethyl ether was added portionwise 5.1 g (0.0194 mole) of triphenylphosphine. This mixture was stirred overnight and was then filtered to remove the solid which had formed, and the solvent was evaporated under reduced pressure. The residue was passed through a column of silica gel. Appropriate fractions were combined, and the solvent was evaporated yielding 1.1 g of N-(4-chloro-2-fluoro-5-bromomethylphenyl)-3,4,5,6tetrahydrophthalimide as a white solid, m .p. 126°-128° C. The nmr and ir spectra were consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04846882 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-aa65f84364d04a1e9bce2fd31f1bed1a |
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| Source note | uspto-grants-1989_07 |
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