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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714589Generated: November 2, 2026

Formaldehyde → 2-[2-[4-(3-Benzyloxyphenylthio)-2-chlorophenyl]ethyl]-2-nitro-1,3-propanediol

https://huagongshe.com/reaction/1714589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
Reactant1,5-Diazabicyclo(4.3.0)non-5-eneHCID 76349—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiazabicyclo(2.2.2)octaneHCID 136165—
Reactant1-Benzyloxy-3-[3-chloro-4-(3-nitropropyl)phenylthio]benzeneHCID 11509867—
SolventAcetonitrileHCID 6342—
Product2-[2-[4-(3-Benzyloxyphenylthio)-2-chlorophenyl]ethyl]-2-nitro-1,3-propanediolHCID 11576483—

Reaction Steps

1-Benzyloxy-3-[3-chloro-4-(3-nitropropyl)phenylthio]benzene (8) is dissolved in an organic solvent, such as acetonitrile and tetrahydrofuran. While the mixture is chilled in an ice bath, a formaldehyde solution is added and the reaction is allowed to proceed at 0 to 60° C. for 1 to 3 hours in the presence of a base, such as 1,8-diazabicyclo[5.4.0]undeca-7-ene, 1,5-diazabicyclo[4.3.0]non-5-ene, diazabicyclo[2.2.2]octane, trialkylamine, sodium hydroxide and potassium hydroxide. Subsequently, the product is treated to give 2-[2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl]-2-nitro-1,3-propanediol (9) or a hydrate thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795472B2
Source datasetuspto-grants-2010_09
ORD IDord-9e11d5610dca4000a6cff8eb442b0183
Source noteuspto-grants-2010_09