HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230122Generated: October 25, 2026
4-(Diethoxymethyl)benzaldehyde → 4-(Hydroxymethyl)benzaldehyde
https://huagongshe.com/reaction/230122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Diethoxymethyl)benzaldehyde | HCID 595993 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(Hydroxymethyl)benzaldehyde | HCID 556330 | 89.4% |
Reaction Steps
To a cold (0° C.) solution of 4-(diethyoxymethyl)benzaldehyde (5.2 g, 24 mmol) in MeOH (50 mL) was added NaBH4 (0.93 g, 24 mmol), and the reaction mixture was stirred for 3 hours. The MeOH was removed and the residue was taken up in DCM and diluted with water. The aqueous layer was extracted with DCM (3×50 mL). The combine organic layers were dried, filtered and concentrated. The crude oil was dissolved in MeOH (50 mL) and cooled to 0° C. To this was added 2N HCl (10.0 mL) in ether. The reaction mixture was left at room temperature for 24 hours. The MeOH was removed and the crude product was purified by flash column chromatography, eluting with EtOAc/Hexane (3:7) to yield 2.92 g of 4-(hydroxymethyl)benzaldehyde (11) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566716B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-ee732d22252346e6b92541f5244d0cef |
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| Source note | uspto-grants-2009_07 |
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