HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410461Generated: October 31, 2026
Methyl 4-Formylbenzoate → Methyl 4-(hydroxy(thiazol-2-yl)methyl)benzoate
https://huagongshe.com/reaction/410461
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(hydroxy(thiazol-2-yl)methyl)benzoate | HCID 12017830 | 96% |
Reaction Steps
2-Bromothiazole (2.72 ml, 30.5 mmol) was taken up in THF (60 ml) and cooled to −20° C. Isopropylmagnesium chloride (16.00 ml, 32.0 mmol) was added drop wise. After stirring for 1 h (−10° C. to 0° C.), the reaction was cooled to −78° C., and methyl 4-formylbenzoate (5.50 g, 33.5 mmol) in THF (10 ml) was added drop wise. The reaction was stirred for 30 min at −78° C., then warmed to room temperature. After 1 h at room temperature, the reaction was quenched with aqueous saturated NH4Cl and extracted with EtOAc (2×). The combined organic layers were dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (10-75% EtOAc/hexanes) to provide methyl 4-[hydroxy(1,3-thiazol-2-yl)methyl]benzoate (7.29 g, 29.2 mmol, 96% yield) as an off-white solid. MS ESI: [M+H]+ m/z 250.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759366B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-3a5c3e5be95548ae9c449e5cdae735a6 |
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| Source note | uspto-grants-2014_06 |
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