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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262745Generated: November 1, 2026

Water → HCID 131713526, compound

https://huagongshe.com/reaction/1262745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiphenylacetyleneHCID 10390—
ReactantHCID 57165332HCID 57165332—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 131713526HCID 131713526—

Reaction Steps

Biphenyl acetylene 5.6 g was dissolved in THF (150 mL) at -78° C. One equivalent n-BuLi was added over one hour. The reaction was allowed to reach room temperature for one hour. 1-Iodo-3-0-tetrahydropyranylpropan-3-ol was added, (one equivalent). The reaction was refluxed for 24 hours. The product 1-0-tetrahydropyranyl-5-(4'-biphenylyl)-pent-4-yn-1-ol, (oil C: 82.47, H: 7.55) was isolated by addition of water and extraction with ethyl acetate. The product (1 g) was dried (60° 10-3 mmHg), dissolved in CH2Cl2 (50 mL) and Ph3P.Br2 (1.95 g) was added, after stirring for 15 minutes at room temperature NaCN (0.54 g) in 20 mL DMSO was added. The mixture was heated at 45° for 16 hours. The intermediate 1-cyano-6-(4'-biphenylyl)pent-5-yne m.p. 60°-61° C.: 88.13, H: 6.16, N: 5.71 was isolated by addition of water and extraction with EtOAc-hydrolysis to the title acid 10 was achieved by refluxing the nitrile in 10 mL (2N NaOH in 50 mL ethanol) followed by acidification with 6N HCl. The product 10 was filtered off and dried, 70% yield. m.p. 95°-96°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04453005
Source datasetuspto-grants-1984_06
ORD IDord-756ca969ae5b4d008ad3b18afb41b4e5
Source noteuspto-grants-1984_06