Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiazole | HCID 9256 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 10774002 | HCID 10774002 | — |
Reaction Steps
In a bomb tube, a mixture of 3.7 g (20 mmol) of 4-bromobenzaldehyde (Fluka, Buchs, Switzerland), 6.64 ml (93 mmol) of thiazole, 2.94 g of potassium acetate and 1.16 g (1 mmol) of Pd(PPh3)4 in 50 ml of dimethylacetamide is stirred at 150° C. for 12 hours. The reaction mixture is concentrated by evaporation. Water is added to the residue and the mixture is extracted 3× with methylene chloride. The organic phases are filtered through cotton wadding, concentrated by evaporation and chromatographed (SiO2 ; hexane/ethyl acetate 1:2), yielding the title compound: HPLC20-100 : tRet =11.4; 1H-NMR (CD3OD) δ 9.98 (s, HCO), 9.03(S, H(2)thiazole), 8.32(S, H(4)thiazole), 7.95 and 7.85 (2d, J=8, each 2H); additionally also signals of the hydrate (≈12%): 8.92(S, H(2)thiazole), 8.15(S, H(4)thiazole), 7.62 and 7.53 (2d, J=8, each 2H), 5.54(S, HC(OH)2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166004 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-5727a585a1924b1eb692dec55cdd2e70 |
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| Source note | uspto-grants-2000_12 |
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