Hydrogen Cyanide → HCID 13309736, compound
Reaction equation
[CH3:1][C:2]1([CH2:9][O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:7][CH2:6][CH:5]=[C:4]([CH3:8])[O:3]1.[CH:18]#[N:19]>N1C=CC=CC=1>[CH3:8][C:4]1([C:18]#[N:19])[CH2:5][CH2:6][CH2:7][C:2]([CH3:1])([CH2:9][O:10][CH2:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[O:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 15.0 g, 3,4-dihydro-2,6-dimethyl-2-[(phenylmethoxy)-methyl]-2H-pyran, 1.75 g liquid hydrogen cyanide, and 0.1 g pyridine sealed in a 30 ml glass bomb was kept at 150° C. for 16 hours. The resulting dark brown solution was distilled (Kugelrohr) to give 15.7 g colorless product, bp 112°-118° C. (0.01 torr), as an isomeric mixture, ca 4:6, cis:trans, based on NMR spectrum in CDCl3.
Workup
- distillationThe resulting dark brown solution was distilled (Kugelrohr)
Sources & evidence
- ORD record
- ord-c51e4bf0012f4051be0cdfd36c06b66a
- Source dataset
- uspto-grants-1985_01
- Patent number
- US04493936
Reaction notes
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