HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49714Generated: October 30, 2026
Hydrochloric Acid → (3-Acetoxy-4-nitro-phenyl)acetic acid
https://huagongshe.com/reaction/49714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(3-Hydroxy-4-nitrophenyl)acetic acid | HCID 23508325 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Acetoxy-4-nitro-phenyl)acetic acid | HCID 17946639 | 519.3% |
Reaction Steps
A stirred mixture of (3-hydroxy-4-nitro-phenyl)acetic acid (1 2.0 g), aqueous sodium hydroxide (152.3 mL, 1M) and diethyl ether (150 mL), cooled to 0° C. in an ice salt bath, was treated dropwise with acetic anhydride (8.1 g) at a rate to maintain the temperature at 0° C. When the addition was complete the mixture was stirred at 0° C. for a further 2 hours then acidified with dilute hydrochloric acid and then extracted with ethyl acetate. The extracts were dried over magnesium sulphate and then evaporated to give the title compound (12.6 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06706738B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-60d046c6b3554acfb33ad147ac87161e |
|---|
| Source note | uspto-grants-2004_03 |
|---|