HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266473Generated: October 30, 2026
Allyl bromide → 2-Benzyl-4-ethoxy-7-allyloxysaccharin
https://huagongshe.com/reaction/266473
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Benzyl-4-ethoxy-7-hydroxysaccharin | HCID 70050549 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-Benzyl-4-ethoxy-7-allyloxysaccharin | HCID 70050921 | 96% |
Reaction Steps
A mixture of 2-benzyl-4-ethoxy-7-hydroxysaccharin (1.0 g), allyl bromide (0.36 g), potassium carbonate (0.62 g) and methyl ethyl ketone (about 20 mL) was heated at 80° C. for one hour. More allyl bromide (0.36 g) was added and heating at 80° C. was continued for one and one-half hours. The mixture was cooled and poured into ice-water (500 mL). The solid was collected affording 2-benzyl-4-ethoxy-7-allyloxysaccharin, 1.08 g, 96% yield, mp 148°-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650422 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-f6f5f57cc48644b99c0a9f1d6e574800 |
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| Source note | uspto-grants-1997_07 |
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