Potassium Hydroxide → HCID 86678286, compound
Reaction equation
[OH:1][CH2:2][C:3]1([NH:6][C:7](=[O:13])[O:8][C:9]([CH3:12])([CH3:11])[CH3:10])[CH2:5][CH2:4]1.[OH-].[K+].Br[CH2:17][CH2:18][CH2:19][P:20](=[O:27])([O:24][CH2:25][CH3:26])[O:21][CH2:22][CH3:23]>C1COCC1.[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[CH2:25]([O:24][P:20]([CH2:19][CH2:18][CH2:17][O:1][CH2:2][C:3]1([NH:6][C:7](=[O:13])[O:8][C:9]([CH3:10])([CH3:12])[CH3:11])[CH2:4][CH2:5]1)([O:21][CH2:22][CH3:23])=[O:27])[CH3:26]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of tert-butyl 1-(hydroxymethyl)cyclopropylcarbamate (1 eq, from the previous step) in THF (0.1 M) at room temperature was added KOH (5 eq), tetrabutylammonium bromide (0.1 eq), and diethyl 3-bromopropylphosphonate (2 eq). The reaction was stirred at room temperature overnight. The mixture was concentrated en vaccuo and then taken up in DCM/water. The aqueous layer was extracted with DCM (2×). The combined organic layers were dried over anhydrous MgSO4, and concentrated en vaccuo. The crude mixture was purified by flash chromatography on a COMBIFLASH® system (ISCO) using a gradient of 0-100% ethyl acetate in hexanes and then 100% ethyl acetate to give the product as an oil.
Workup
- concentrationThe mixture was concentrated en vaccuo
- extractionThe aqueous layer was extracted with DCM (2×)
- dry with materialThe combined organic layers were dried over anhydrous MgSO4
- concentrationconcentrated en vaccuo
- customThe crude mixture was purified by flash chromatography on a COMBIFLASH® system (ISCO)
Sources & evidence
- ORD record
- ord-1b4689ab1c0f4c1ab54078ee21b7d97d
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365506B2
Reaction notes
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