HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromobutane → HCID 85871665, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | Benzyl 2-pyridin-4-ylacetate | HCID 11413519 | — |
| Product | HCID 85871665 | HCID 85871665 | — |
Reaction Steps
Benzyl 4-pyridylacetate (Step B, 0.80 g, 3.5 mmol) was reacted with potassium hydride and 1,4-dibromobutane according to the procedures described in Example 33, Step A to afford the title compound. 1H NMR (400 MHz, CD3OD): 8.42 (d, 2H), 7.39 (d, 2H), 7.28 (m, 3 H), 7.19 (m, 2H), 5.06 (s, 2H), 2.62 (m, 2H), 1.97 (m, 2H), 1.74 (m, 4H). LC-MS: m/e 282 (M+H)+ (2.2 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423067B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-86d86d8b5cf24ef2aaa629901c0d9ebe |
| Source note | uspto-grants-2008_09 |