HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441928Generated: November 1, 2026
6-Hydroxyquinoline → HCID 11573719, compound
https://huagongshe.com/reaction/1441928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Hydroxyquinoline | HCID 11374 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromophenyl isocyanate | HCID 141001 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11573719 | HCID 11573719 | — |
Reaction Steps
A solution of quinolin-6-ol (0.29 g., 2 mmol) in dry dimethylformamide (3 ml) was added to a stirred suspension of sodium hydride (0.048 g., 2 mmol) in dry dimethylformamide (2 ml) at −10° C. during 5 min. The reaction mixture was stirred for ½ hours. Then 3-bromo-phenyl isocyanate (0.475 g., 2.4 mmol) was added to the stirring reaction mixture. Stirring was continued for additional 1 hr. during which the temperature was allowed to rise to room temperature (21° C.). The reaction mixture was quenched with water (0.2 ml), diluted with water (2 ml), extracted with ethyl acetate (2×5 ml) and dried over sodium sulphate. The combined fractions of ethyl acetate were concentrated under vaccum. The residue was washed with methanol (2×2 ml) to give 1d; yield: 0.35 g. (51.01%), m.p. 260° C., C16H11BrN2O2; 1H NMR δ ppm (pyridine d5): 7.09-7.58 (m, 9H), 8.28 (bs, 2H), 9.58 (bs, 1H); IR vmax (KBr) (cm−1). 522, 645, 743, 782, 877, 928, 992, 1069, 1227, 1286, 1406, 1470, 1581, 1637, 1875, 1946, 2374, 3290, 3753, 3872, 3952.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655801B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-81681b09f0fc4550801580fe5f0f8824 |
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| Source note | uspto-grants-2010_02 |
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