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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963770Generated: October 30, 2026

Formaldehyde → HCID 19082710, compound

https://huagongshe.com/reaction/963770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86752771HCID 86752771—
CatalystAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductHCID 19082710HCID 19082710—

Reaction Steps

Paraformaldehyde (750 mg, 25 mmol) and DBU (1.85 ml, 12.4 mmol) were added to a solution of 2-nitrobenzylmethylether (4.18 g, 25 mmol) in DMSO (3.5 ml, synthesis quality, additionally dried for 2 d over molecular sieve 4 Å) and allowed to react at room temperature for 4 h. The pH value was adjusted from pH 9 to about pH 3.5 by means of a few drops of conc. AcOH. The mixture was diluted with CH2Cl2 (120 ml) and washed with H2O (80 ml). The aqueous phase was post-extracted with CH2 Cl2 (2×80 ml). The combined organic phases were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product (5.56 g) was purified by column chromatography (140 g SiO2, 21×4.2 cm, solvent: toluene 300 ml, toluene/EtOAc 20:1 210 ml, 15:1 160 ml, 10:1 220 ml, 15:2 170 ml, 6:1 210 ml, 5:1 180 ml, 4:1 400 ml, 3:1 240 ml, 2:1 240 ml). First 2-nitrobenzylmethylether (2.442 g, 58%) was eluted then 2-methoxy-2-(2-nitrophenyl)ethanol (1.696 g, 34% and 82% respectively, in relation to the consumed starting material).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763599
Source datasetuspto-grants-1998_06
ORD IDord-ceeeaa01865c4ed2a2e4c2a0b1cde0bf
Source noteuspto-grants-1998_06