HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368817Generated: October 26, 2026
Sodium Iodide → 1-(2-Cyanoethyl)isochroman
https://huagongshe.com/reaction/368817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(2-Chloroethyl)isochroman | HCID 10607966 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Cyanoethyl)isochroman | HCID 14203071 | — |
Reaction Steps
A mixture of 1-(2-chloroethyl)isochroman (LXIV, PREPARATION 2, 0.9874 g, 5.02 mmol), sodium cyanide (0.3793 g, 7.74 mmol), sodium iodide (a few mg) and DMF (5 ml) is heated overnight at 85°. Additional sodium cyanide (0.5826 g, 11.9 mmol) is then added in two portions, along with DMF (14 ml) and a few mgs of sodium iodide. The mixture is heated at 97° for another two days and then cooled and poured into water. The mixture is extracted several times with ethyl acetate and the combined organic phase is backwashed twice with water, followed by two saline washes, then dried over magnesium sulfate and concentrated to dryness. The crude product is chromatographed on silica gel eluting with ethyl acetate/hexane (10/90). The appropriate fractions are pooled and concentrated to give 1-(2-cyanoethyl)isochroman (LXXXVI), NMR (CDCl3) 2.11, 2.27-2.72, 2.98, 3.77, 4.13, 4.86 and 7.17 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133446 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-6f0c80c6796f4e8e8c7031c7bbf12f24 |
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| Source note | uspto-grants-2000_10 |
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