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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977276Generated: October 31, 2026

Acetic Anhydride → HCID 19965633, compound

https://huagongshe.com/reaction/977276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium CyanideHCID 8929—
ReactantHCID 19965659HCID 19965659—
CatalystBenzyltributylammonium chlorideHCID 159952—
SolventDichloromethaneHCID 6344—
ProductHCID 19965633HCID 19965633—

Reaction Steps

After a mixture of 5-[4-[2-[2-(2-furyl)-5-methyl-4-oxazolyl]ethyl]phenyl]pentan-1-al (2.2 g), sodium cyanide (0.383 g), acetic anhydride (0.796 g), benzyltributylammonium chloride (0.608 g) and dichloromethane (40 ml)water (10 ml) was stirred at room temperature for 2 hours, the organic layer was separated, washed with water, dried (MgSO4), and then concentrated under reduced pressure, to yield 2-acetoxy-6-[4-[2-[2-(2-furyl)-5-methyl-4-oxazolyl]ethyl]phenyl]hexanenitrile as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614544
Source datasetuspto-grants-1997_03
ORD IDord-566b297a4e58421b899fb78c9db97a2b
Source noteuspto-grants-1997_03