Hydrochloric Acid → HCID 86676834, compound
Reaction equation
[OH-].[CH2:2]([N+:8]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH3:27][O:28][C:29](=[O:32])[O:30]C.Cl.COC(=O)[O-]>CO.CC(O)C>[CH3:27][O:28][C:29](=[O:30])[O-:32].[CH2:21]([N+:8]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]Participants
7
Procedure
10 g of a 10% b.w. solution of tetrahexylammonium hydroxide (2.7 mmole) in methanol was mixed with 1 g (11 mmoles) of dimethylcarbonate (DMC) to yield a clear, colorless solution. Titration in 2-propanol with aqueous HCl after 24 hours revealed an equivalence point at a lower pH for the blocked versus the unblocked form and indicated complete blocking to 0.26 meq methylcarbonate per g solution.
Workup
- customto yield a clear, colorless solution
Sources & evidence
- ORD record
- ord-99384695ad134670ae6c07482d09b26e
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181452B2
Reaction notes
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