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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072351Generated: November 3, 2026

Sodium Cyanide → (R)-(+)-4-tert. butoxy-3-methylbutyronitrile

https://huagongshe.com/reaction/2072351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactantbromo ether (S)-(+)-3-tert. butoxy-2-methyl-1-bromopropaneHCID 86735108—
SolventWaterHCID 962—
Product(R)-(+)-4-tert. butoxy-3-methylbutyronitrileHCID 1292332166.2%

Reaction Steps

A mixture of 23.1 g. (0.11 mole) of bromo ether (S)-(+)-3-tert. butoxy-2-methyl-1-bromopropane and 11.07 g. (0.225 mole) of sodium cyanide in 144 ml. of water was stirred and refluxed for 17 hours. After cooling, the reaction mixture was diluted with water and worked up by extraction with CH2Cl2 in the manner of Example 1. The crude product was chromatographed on 500 g. of silica gel. Elution with 9:1 parts by volume and 4:1 parts by volume hexane-ether followed by evaporative distillation gave (R)-(+)-4-tert. butoxy-3-methylbutyronitrile (11.3 g.; 64.5%) as a colorless liquid, b.p. 88°-90° C. (bath temperature) (11 mm Hg.); [α]25D + 7.41° (c 1.8, C6H6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04051153
Source datasetuspto-grants-1977_09
ORD IDord-8ab9029872194038910eb0ca0ca349b6
Source noteuspto-grants-1977_09