HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2,3-Dihydro-1,4-benzodioxin-6-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 6-(Chloromethyl)-2,3-dihydro-1,4-benzodioxine | HCID 5230287 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(2,3-Dihydro-1,4-benzodioxin-6-yl)acetonitrile | HCID 4737346 | 86% |
Reaction Steps
A mixture of 6-chloromethyl-2,3-dihydro-benzo[1,4]dioxine (12.5 g, 67.7 mmol) and NaCN (4.30 g, 87.8 mmol) in DMSO (50 mL) was stirred at rt for 1 h. The mixture was poured into water (150 mL) and then extracted with dichloromethane (50 mL×4). The combined organic layers were washed with water (50 mL×2) and brine (50 mL), dried over Na2SO4 and concentrated to dryness. The residue was purified by column (Petroleum Ether/Ethyl Acetate 50:1) on silica gel to obtain 2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)acetonitrile as a yellow oil (10.2 g, 86%). 1H-NMR (300 MHz, CDCl3) δ 6.78-6.86 (m, 3H), 4.25 (s, 4H), 3.63 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741933B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-2b35e435066a4714aa0fa0f6b31571c8 |
| Source note | uspto-grants-2014_06 |