HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417625Generated: October 26, 2026
Acetic Acid → 1-(4-Nitrophenyl)-2-nitro-1,3-propanediol
https://huagongshe.com/reaction/2417625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Nitroethanol | HCID 22056827 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(4-Nitrophenyl)-2-nitro-1,3-propanediol | HCID 13468905 | 70.24% |
Reaction Steps
7.55 g (0.05 moles) of 4-nitrobenzaldehyde and 4.55 g (0.05 moles) of nitroethanol are suspended in a mixture of 30 ml of methanol and 0.2 ml of triethylamine. The mixture is stirred at 0° C. until dissolution (about 30 minutes) and then allowed to stand at 0° C. for 20 hours. The mixture is acidified (pH 2) with 0.2 ml of acetic acid and 0.2 ml of concentrated hydrochloric acid, and 20 ml of ice-cold water are added. The separated crystals are filtered off, washed with chloroform and dried. 8.5 g (70.24%) of 1-(4-nitrophenyl)-2-nitro-1,3-propanediol are obtained; m.p. 105°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04469703 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-bc6d5460c6434353ba32bf5d9543c3fd |
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| Source note | uspto-grants-1984_09 |
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