HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382850Generated: October 30, 2026
Acetic Anhydride → Butyl 2-methylene-3-acetoxy-4,4,4-trichlorobutyrate
https://huagongshe.com/reaction/382850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 18362110 | HCID 18362110 | — |
| Catalyst | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Butyl 2-methylene-3-acetoxy-4,4,4-trichlorobutyrate | HCID 11220844 | 91.4% |
Reaction Steps
To 1173.0 g of butyl 2-methylene-3-hydroxy-4,4,4-trichlorobutyrate (91% pure) charged in a 2-liter, 3-neck round bottom flask equipped with a mechanical stirrer, thermometer, and a condenser were added 520.0 g of acetic anhydride and 7.0 g of sodium acetate. The reaction mixture was heated at 120° C. for three hours. Unreacted acetic anhydride and formed acetic acid were stripped off under vacuum at <80° C./0.6 mm Hg. After cooling to room temperature, the solid sodium acetate that had settled to the bottom of the flask was separated. 1236.1 g of acetylated product was obtained, 91.3% purity (GC analysis), 91.4% yield. The product structure was confirmed by NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310237B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-457871aa308a437d8d54dc4a146eb30b |
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| Source note | uspto-grants-2001_10 |
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