HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 5-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran | HCID 11745437 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran | HCID 66760928 | 86% |
Reaction Steps
N-bromosuccinimide (12.5 g, 70.0 mmol) was added to a solution of acetonitrile (165 mL) containing 2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran (11.1 g, 58.3 mmol) synthesized in Reference Example 3 under ice-cooling condition, and the mixture was warmed to room temperature. After stirring for 5 hours, water was added to the reaction solution. The generated precipitate was collected by filtration and washed with a mixture of acetonitrile/water (1/2). The solid was dried to give 13.5 g of the title compound (yield: 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957069B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-68e6d64275b441dc99a0b8d2cc5cc951 |
| Source note | uspto-grants-2015_02 |