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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417798Generated: October 27, 2026

Sodium Iodide → 1-(2-Cyanoethyl)isochroman

https://huagongshe.com/reaction/1417798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantSodium CyanideHCID 8929—
Reactant1-(2-Chloroethyl)isochromanHCID 10607966—
SolventWaterHCID 962—
Product1-(2-Cyanoethyl)isochromanHCID 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 856. 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 (LXVI), NMR (CDCl3) 2.11, 2.27-2.72, 2.98, 3.77, 4.13, 4.86 and 7.17 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877317
Source datasetuspto-grants-1999_03
ORD IDord-d7fad628c72a4afbaeb72d3f8a753287
Source noteuspto-grants-1999_03