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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723982Generated: October 30, 2026

Sodium Cyanide → HCID 178519557, compound

https://huagongshe.com/reaction/723982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant[3-(Tert-butyl-dimethyl-silanyloxymethyl)-cyclohex-3-enyl]-acetaldehydeHCID 131726104—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178519557HCID 178519557—

Reaction Steps

The following preparation followed the procedure by Horne et al., Heterocycles 39:139 (1994). A solution of the aldehyde (Intermediate R5; 0.34 g, 1.3 mmol) in EtOH (5 mL) was treated with tosylmethyl isocyanide (TosMIC; Aldrich; 0.25 g; 1.3 mmol) and NaCN (˜15 mg, cat) and allowed to stir at room temperature for 20 minutes. The solvent was removed in vacuo; the residue was dissolved in ˜7M NH3 in MeOH and transferred to a resealable tube before heating at 100° C. for 15 hours. The mixture was concentrated and purified by chromatography on SiO2 with 5% MeOH (sat. w/NH3):CH2Cl2. A solution of the product in THF with TBAF (1.5 eq.) was stirred at room temperature after aqueous workup. The crude product was chromatographed (5–7% NH3/MeOH in CH2Cl2) and designated Compound 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141597B2
Source datasetuspto-grants-2006_11
ORD IDord-89b6b05368464569a4d89aef99cd1f92
Source noteuspto-grants-2006_11