(2-Methylpropyl)boronic acid → (3aS,4S,6S,7aR)-3a,5,5-Trimethyl-2-(2-methylpropyl)hexahydro-2H-4,6-methano-1,3,2-benzodioxaborole

HRID 2103977Notes

Reaction equation

HRID 2103977 reaction equation
[C:1]12(O)[CH2:9][CH:5]([C:6]1([CH3:8])[CH3:7])[CH2:4][CH2:3][C:2]2([OH:11])[CH3:10].[CH3:13][CH:14]([CH3:19])[CH2:15][B:16](O)[OH:17]>C(OCC)C>[CH3:13][CH:14]([CH3:19])[CH2:15][B:16]1[O:17][C@@H:3]2[CH2:4][C@@H:5]3[CH2:9][C@H:1]([C@:2]2([CH3:10])[O:11]1)[C:6]3([CH3:8])[CH3:7]

Participants

4

Reactant 2

HCID 2734395(2-Methylpropyl)boronic acidHCID 219250472,6,6-Trimethylbicyclo[3.1.1]heptane-1,2-diol

Product 1

HCID 12842239(3aS,4S,6S,7aR)-3a,5,5-Trimethyl-2-(2-methylpropyl)hexahydro-2H-4,6-methano-1,3,2-benzodioxaboroleYield 98.6%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

A mixture of (+)-pinanediol (23.9 g, 0.140 mol) and 2-methylpropylboronic acid (15 g, 0.147 mol) in diethyl ether (300 ml) was stirred at room temperature for 24 h. The mixture was dried over anhydrous sodium sulfate and purified by column chromatography (Silica gel 230-400 mesh), eluting with hexane:ethyl acetate 90:10 mixture. The product was obtained as a clear oil (32.6 g, 94% yield).

Workup

  1. dry with materialThe mixture was dried over anhydrous sodium sulfate
  2. custompurified by column chromatography (Silica gel 230-400 mesh)
  3. washeluting with hexane:ethyl acetate 90:10 mixture

Sources & evidence

ORD record
ord-4e5ad38430984ce5bee855a1cb40abf1
Source dataset
uspto-grants-2009_08
Patent number
US07576206B2

Reaction notes

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