HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-[2-[4-(3-Benzyloxyphenylthio)-2-chlorophenyl]ethyl]-2-nitro-1,3-propanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,5-Diazabicyclo(4.3.0)non-5-ene | HCID 76349 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Diazabicyclo(2.2.2)octane | HCID 136165 | — |
| Reactant | 1-Benzyloxy-3-[3-chloro-4-(3-nitropropyl)phenylthio]benzene | HCID 11509867 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[2-[4-(3-Benzyloxyphenylthio)-2-chlorophenyl]ethyl]-2-nitro-1,3-propanediol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795472B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-9e11d5610dca4000a6cff8eb442b0183 |
| Source note | uspto-grants-2010_09 |