HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371652Generated: October 30, 2026
Acetic Anhydride → HCID 20355562, compound
https://huagongshe.com/reaction/371652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Bromoethene | HCID 11641 | — |
| Reactant | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20355562 | HCID 20355562 | 49% |
Reaction Steps
Magnesium metal (5 g., 0.206 mole) is suspended in tetrahydrofuran (100 ml.) in a three-necked, round-bottomed flask protected by a dry ice condenser and equipped with a mechanical stirrer. The stirrer is started and vinyl bromide (22 g., 0.206 mole) in tetrahydrofuran is added at such a rate as to keep the solvent refluxing. The reaction mixture is refluxed for 0.5 hours after the addition is complete. The reaction mixture is then cooled to 0°-5° C. and benzyloxyacetaldehyde (24 g., 0.16 mole) in tetrahydrofuran (15 ml.) is added dropwise. After 1.5 hours at 0°-5° C., there is added acetic anhydride (26 g., 0.255 mole) and the reaction mixture is allowed to come to room temperature. After 20 hours at room temperature, ice water (500 ml.) is added and the product is extracted into ethyl acetate (3 × 100 ml.). The ethyl acetate extract is washed with brine, dried (Na2SO4), and distilled. There is obtained 17 g. (49%) of the title compound, b.p. 85°-95° C./0.05 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04087435 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-59e1b5590e544819943c0a79f7451506 |
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| Source note | uspto-grants-1978_05 |
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