HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487827Generated: October 27, 2026
3-Formyl-4-methylbenzoic acid → 3-(1-Hydroxy-3-buten-1-yl)-4-methylbenzoic acid
https://huagongshe.com/reaction/1487827
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Formyl-4-methylbenzoic acid | HCID 19019191 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-Hydroxy-3-buten-1-yl)-4-methylbenzoic acid | HCID 90066678 | 95.4% |
Reaction Steps
Into a 100-mL 3-necked round-bottom flask, which was purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-formyl-4-methylbenzoic acid (compound 4.1, 2.00 g, 12.2 mmol) in tetrahydrofuran (50 mL). The mixture was cooled to −10 to 0° C. then allylmagnesium bromide (1M in Et2O, 24.4 mL, 24.4 mmol) was added drop-wise. The resulting mixture was stirred for 1 hr at −10-0° C., then carefully quenched with saturated aqueous NH4Cl (50 mL) and diluted with ethyl acetate (200 mL). The organic layer was washed with saturated aqueous NH4Cl (80 mL) and brine (2×80 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to yield the title compound as a light red solid (2.4 g, crude), which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-57b4d753a52d4121acb42c40ac095142 |
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| Source note | uspto-grants-2016_08 |
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