HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430236Generated: October 31, 2026
Acetic Acid → Benzenemethanol, 2-(dimethylamino)-
https://huagongshe.com/reaction/1430236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | m-(Dimethylamino)benzyl alcohol | HCID 90133 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzenemethanol, 2-(dimethylamino)- | HCID 138325 | — |
Reaction Steps
In a 250 mL round-bottomed flask, (3-(dimethylamino)phenyl)methanol (1 g) and paraformaldehyde (2.5 g) were added to acetic acid (150 mL) to give a suspension. Sodium cyanoborohydride (2.6 g) was added slowly. The mixture was stirred at room temperature overnight. After concentration of the solvent, water and ethyl acetate (1:1, 100 mL) were added. After separation, the aqueous layer was extracted by ethyl acetate (2×20 mL). The combined organic layers were washed with water (3×50 mL), saturated aqueous NaHCO3 (2×30 mL), and dried over Na2SO4. After filtration and concentration, the residue was taken up into CH2Cl2 and the product was purified by flash chromatography (Varian, Superflash SF40-80 g column), eluting with 0-20% methanol/dichloromethane, to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940737B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-54344432f25f49ab9b35b459c9a22522 |
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| Source note | uspto-grants-2015_01 |
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