Potassium Carbonate → HCID 23507944, compound

HRID 2289232Notes

Reaction equation

HRID 2289232 reaction equation
C[Si](C)(C)[C:3]#[C:4][C:5]1[CH:14]=[C:13]2[C:8]([CH2:9][CH2:10][C:11]3([O:18][CH2:17][CH2:16][O:15]3)[CH2:12]2)=[CH:7][CH:6]=1.C([O-])([O-])=O.[K+].[K+]>CO>[C:4]([C:5]1[CH:14]=[C:13]2[C:8]([CH2:9][CH2:10][C:11]3([O:15][CH2:16][CH2:17][O:18]3)[CH2:12]2)=[CH:7][CH:6]=1)#[CH:3]

Participants

4

Procedure

A solution of 3', 4'dihydro-7'[2-(trimethylsilyl)ethynyl]spiro[1,3-dioxolane-2,2'(1'H)-naphthalene](1.45 g, 5.02 mmol ) and suspended K2CO3 (0.50 g) in methanol (20 ml) was stirred at room temperature for 30 minutes. The solution was then filtered and concentrated in vacuo. The residue was absorbed onto silica gel (2 g) and purified by chromatography on silica gel (1 hg) eluting with diethyl ether:hexane (1:9) to give 7'-ethynyl-3', 4'-dihydrospiro[1,3-dioxolane-2,2'(1'H)-naphthalene] as a solid (0.85 g). 1H NMR (CDCl3, 200 MHz) δ: 1.94 (t, J=7 Hz, 2H, CH2), 2.95 (s, 2H, CH2), 2.98 (t, J=7 Hz, 2H, CH2), 3.01 (s, 1H, ethynyl H), 4.02 (s, 4H, OCH2CH20), 7.07 (d, J=8 Hz, 1H, Ar), 7.19 (s, 1H, Ar), 7.24 (d, J=8 Hz, 1H, Ar).

Workup

  1. filtrationThe solution was then filtered
  2. concentrationconcentrated in vacuo
  3. customThe residue was absorbed onto silica gel (2 g)
  4. custompurified by chromatography on silica gel (1 hg)
  5. washeluting with diethyl ether:hexane (1:9)

Sources & evidence

ORD record
ord-4780425570c84a48bb6521ec4273b564
Source dataset
uspto-grants-2000_07
Patent number
US06090941

Reaction notes

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