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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971149Generated: October 28, 2026

Acetic Acid → HCID 44581496, compound

https://huagongshe.com/reaction/971149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 44581495HCID 44581495—
CatalystAcetoneHCID 180—
SolventAcetonitrileHCID 6342—
ProductHCID 44581496HCID 4458149651%

Reaction Steps

The product from Example 130 (30 mg, 0.066 mmol) was stirred in CH3CN (0.2 mL) at rt under N2. Aqueous formaldehyde (0.07 mL, 7 mmol, 10 eq) was added followed by the addition of HOAc (0.012 mL, 0.21 mmol, 3.2 eq). The mixture was stirred for 15 min, and then NaBH3CN (12 mg, 0.198 mmol) was added. The mixture was stirred at rt for 2 h. Several drops of acetone were added followed by 1N NaOH. The mixture was extracted with CH2Cl2, washed with H2O and brine, dried over MgSO4, and concentrated to dryness. The residue was purified by FCC (silica gel, EtOAc, than EtOAc:MeOH=10:1) to yield the title compound (15.7 mg, 51%). 1H NMR (CDCl3) δ 7.46 (d, J=8.8 Hz, 2H), 7.29 (m, 4H), 6.92 (d, J=9.2 Hz, 2H), 4.15 (t, J=6.6 Hz, 2H), 3.81 (s, 3H), 3.16 (t, J=6.6 Hz, 2H), 2.28 (s, 6H), 1.02 (m, 2H), 0.81 (m, 2H) ppm. LC/MS (ESI+) 471.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312214B2
Source datasetuspto-grants-2007_12
ORD IDord-47f4d85d5779489eb00f1440241106ab
Source noteuspto-grants-2007_12