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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461996Generated: October 30, 2026

Acetonitrile → HCID 54534630, compound

https://huagongshe.com/reaction/461996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantButyllithiumHCID 178418339—
ProductHCID 54534630HCID 54534630—

Reaction Steps

In this preparation 10 ml. of acetonitrile is stirred in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, and cooled to -70° C. 62.5 Ml. (0.1 mole) of 1.6 M butyl lithium, in hexane, is added dropwise at a controlled rate such that the temperature of the mixture does not exceed -50° C. The mixture is then stirred for five minutes and 0.1 mole adamant-2-one in 60 ml. of anhydrous tetrahydrofuran is added dropwise and the mixture then allowed to warm to room temperature. The mixture is then evaporated, under vacuum, to remove the tetrahydrofuran solvent and then 300 ml. of ethyl acetate is added, and the mixture washed twice with water. The organic layer is separated and dried with anhydrous magnesium sulfate and filterd. The filtrate is evaporated to dryness, under vacuum, affording 2-hydroxy-2-(adamant-2-yl) acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064258
Source datasetuspto-grants-1977_12
ORD IDord-37cf18ec53474041b43bc7d902239cdf
Source noteuspto-grants-1977_12