HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → [3-(5-Bromothien-2-yl)-4,5-dihydroisoxazol-5-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | N-[(5-bromothiophen-2-yl)methylidene]hydroxylamine | HCID 200491 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(5-Bromothien-2-yl)-4,5-dihydroisoxazol-5-yl]methanol | HCID 17954475 | — |
Reaction Steps
5-Bromo-thiophene-2-carbaldehyde oxime (40.2 g, 195.2 mmol) and allyl alcohol (32.4 ml) were added to tetrahydrofuran (200 ml) and then bleach (1318 ml) was added. The reaction was stirred for four hours followed by extraction with tetrahydrofuran (2×200 ml). The organic layers were combined, dried over sodium sulfate, and concentrated in vacuo to give the desired product (19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396847B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-559ae188f9b84d10bd02bb3c32e997cc |
| Source note | uspto-grants-2008_07 |