HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656455Generated: November 1, 2026
Methyl 2-formylbenzoate → HCID 86747309, compound
https://huagongshe.com/reaction/1656455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-formylbenzoate | HCID 243003 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 15035999 | HCID 15035999 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86747309 | HCID 86747309 | 69.9% |
Reaction Steps
A solution of 0.142 g of zinc chloride and 0.065 g of sodium cyanoborohydride in 3 ml of methanol was added to a solution of 0.40 g of trans-4-amino-6-heptafluoropropylsulfonyl-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-ol (prepared as described in Preparation 4) and 0.156 g of methyl 2-formylbenzoate in 6 ml of methanol, and the resulting mixture was stirred at room temperature for 1 hour and then at 50° C. for 24 hours. At the end of this time, the mixture was cooled with ice and then mixed with a saturated aqueous solution of sodium hydrogencarbonate. The methanol was then removed by distillation under reduced pressure, and the resulting residue was diluted with water and extracted with methylene chloride. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, and dried over anhydrous magnesium sulfate; the solvent was then removed by distillation under reduced pressure. The resulting residue was recrystallized from ethyl acetate, to afford 0.356 g of the title compound, melting at 241°-249° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05254578 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-32d00eefdd334747ac19c81428764eaa |
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| Source note | uspto-grants-1993_10 |
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