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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479311Generated: November 2, 2026

Formaldehyde → HCID 46220204, compound

https://huagongshe.com/reaction/1479311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86699633HCID 86699633—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
ProductHCID 46220204HCID 4622020497.4%

Reaction Steps

Compound 1 (4.00 g, 6.67 mmol) obtained in Example 1 was dissolved in 1,2-dichloroethane (50 mL) and methanol (50 mL), and stirred at room temperature for 1 hour after adding formaldehyde (4.96 mL, 66.7 mmol) and sodium triacetoxyborohydride (Acros Organics; 7.06 g, 33.3 mmol). The reaction mixture was further stirred at room temperature for 2.5 hours after adding sodium triacetoxyborohydride (Acros Organics; 7.06 g, 33.3 mmol). The aqueous layer was extracted with ethyl acetate after adding a saturated sodium bicarbonate aqueous solution to the reaction solution. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure after filtration. The resulting residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 95/5) to give compound 10 (3.99 g, 97.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408914B2
Source datasetuspto-grants-2016_08
ORD IDord-a6d329dc42cb4fb9bea0c023247e604a
Source noteuspto-grants-2016_08