HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-6-(1,3-dioxoisoindolin-2-yl)hexanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1,3-Dihydro-1,3-dioxo-2H-isoindole-2-hexanoic acid | HCID 78185 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-6-(1,3-dioxoisoindolin-2-yl)hexanoic Acid | HCID 13622640 | 91.9% |
Reaction Steps
Treat dropwise a mixture of 6-phthalimidocaproic acid (12.7 g, 48 mmol) and dry red phosphorous (1.95 g, 63 mmol) with bromine (12.7 mL, 246 mmol) at 0° C. Warm the resulting lumpy mixture to room temperature and heat to 80° C. for 3 hours. Cool the reaction mixture to room temperature, pour into water (300 mL) containing NaHSO3, and neutralize using solid NaHCO3. Wash the aqueous layer with diethyl ether (150 mL) and acidify with concentrated hydrochloric acid. Collect the pale yellow precipitate by filtration and dry to give 2-bromo-6-phthalimidocaproic acid (15 g, 91.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953788B1 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-4994cd6bab324fcc93d3c5d25da9512c |
| Source note | uspto-grants-2005_10 |