HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809808Generated: October 30, 2026
Water → [2-(3-Methoxy-propoxy)-4-methyl-phenyl]-methanol
https://huagongshe.com/reaction/1809808
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(3-Methoxypropoxy)-4-methylbenzaldehyde | HCID 86053432 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-(3-Methoxy-propoxy)-4-methyl-phenyl]-methanol | HCID 67542816 | — |
Reaction Steps
To a solution of the title B compound, 2-(3-methoxy-propoxy)-4-methyl-benzaldehyde (3.7 g, 17.41 mmol) in 30 mL of methanol is added portion wise sodium borohydride (1.03 g, 26.12 mmol). The reaction mixture is stirred for 30 min at room temperature. Sodium borohydride (1.03 g, 26.12 mmol) is added and the mixture further stirred overnight to complete the reaction. After addition of H2O, the aqueous layer is extracted twice with ethyl acetate. The combined organic extracts are dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by flash column chromatography on silica gel (hexane/EtOAc 4/1 to 1/2) to afford the title compound as a colorless oil: TLC, Rf (hexane/AcOEt 2/1)=0.2. Rt (HPLC, Nucleosil C18, 10:90-100:0 CH3CN/H2O+0.1% TFA within 5 min, then 100% CH3CN+0.1% TFA): 4.88 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362040B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-536b0e60212848bb92409862afa0bbd4 |
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| Source note | uspto-grants-2013_01 |
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