Hydrochloric Acid → HCID 86706068, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1([CH:11](OS(C2C=CC(C)=CC=2)(=O)=O)[CH3:12])[CH2:10][O:9][CH2:8][CH2:7][O:6]1)=[O:4].Cl.C(OCC)C>N1(C2CCCCCCCCCC2)CCCN=CCCCCC1>[CH3:1][O:2][C:3]([C:5]1([CH:11]=[CH2:12])[CH2:10][O:9][CH2:8][CH2:7][O:6]1)=[O:4]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-[1-(toluene-4-sulfonyloxy)-ethyl]-[1,4]dioxane-2-carboxylic acid methyl ester (1.68 g, 4.9 mmol) in 1,8-diazabicycloundec-7-ene (3 mL) was heated in a sealed tube at 130° C. for 2 h. The reaction mixture was cooled to room temperature and 2 M hydrochloric acid and diethyl ether were added. The mixture was extracted with diethyl ether and the organic extracts were combined and washed with brine. The organic solution was filtered through a hydrophobic frit and the filtrate was evaporated. The residue was purified by silica gel chromatography using a gradient of pentane/diethyl ether 3:1 to 1:1 to afford the title compound (308 mg, 36%) as a volatile, colorless oil. 1H NMR (300 MHz, CDCl3) δ 3.47 (d, J=11.6 Hz, 1H), 3.62-3.78 (m, 2H), 3.81-3.86 (m, 1H), 3.84 (s, 3H), 3.99-4.07 (m, 1H), 4.33 (d, J=11.6 Hz, 1H), 5.34 (dd, J=10.7, 1.1 Hz, 1H), 5.52 (dd, J=17.4, 1.1 Hz, 1H), 5.79 (dd, J=17.4, 10.7 Hz, 1H). LCMS (m/z) 195.1 [M+Na], Tr=1.23 min.
Workup
- extractionThe mixture was extracted with diethyl ether
- washwashed with brine
- filtrationThe organic solution was filtered through a hydrophobic frit
- customthe filtrate was evaporated
- customThe residue was purified by silica gel chromatography
Sources & evidence
- ORD record
- ord-03978c9c37614121af62ea481cc45a6a
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062092B2
Reaction notes
Loading…