HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(3,4,5-Trimethoxyphenyl)-2-nitro-1,3-propanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | Nitroethanol | HCID 22056827 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | N-Methylpiperidine | HCID 12291 | — |
| Product | 1-(3,4,5-Trimethoxyphenyl)-2-nitro-1,3-propanediol | HCID 13468887 | — |
Reaction Steps
19.6 g (0.1 moles) of 3,4,5-trimethoxybenzaldehyde and 9.1 g (0.1 moles) of nitroethanol are suspended in a mixture of 25 ml of methanol and 1 ml of N-methylpiperidine at a temperature of 0° C. (under cooling with ice water). The reaction mixture is stirred for 6 hours, then 50 ml of chloroform are added, the mixture is allowed to stand at 0° C. for 72 hours and then acidified with 1 ml of acetic acid. The separated crystalline substance is filtered off, washed with chloroform and ice-cold (0° C.) water and dried. 19.7 g 68.64%) of 1-(3,4,5-trimethoxyphenyl)-2-nitro-1,3-propanediol are obtained; m.p.: 155°-159° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04469703 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-5802cf88c82f4a039286fd237ccba50f |
| Source note | uspto-grants-1984_09 |