Sodium hydride → HCID 59253200, compound
Reaction equation
[H-].[Na+].[OH:3][CH2:4][C:5]([CH3:11])([CH3:10])[C:6]([O:8][CH3:9])=[O:7].Br[CH2:13][CH2:14][O:15][CH3:16]>CN(C=O)C>[CH3:16][O:15][CH2:14][CH2:13][O:3][CH2:4][C:5]([CH3:11])([CH3:10])[C:6]([O:8][CH3:9])=[O:7]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium hydride (60% wt in oil) (3.14 g, 78 mmol) was added to a stirred solution of methyl 3-hydroxy-2,2-dimethylpropanoate (5 mL, 39.2 mmol) in DMF (5.6 mL) at 0° C., after 5 min 1-bromo-2-methoxyethane (7.4 mL, 78 mmol) was added dropwise, and the reaction mixture was allowed to stir for 3 h. The reaction was quenched with sat. NH4Cl (aq.) (30 mL) and the aqueous layer was extracted with DCM (2×50 mL), the combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. The crude oil was dissolved in EtOAc (125 mL) and washed with water (3×40 mL), dried (MgSO4), filtered and concentrated in vacuo. The material was purified by vacuum distillation (68-69° C., 4.4 mbar) to afford methyl 3-(2-methoxyethoxy)-2,2-dimethylpropanoate (39) (1.83 g, 25%) as a colourless oil: 1H NMR (400 MHz, CDCl3) δ: 3.68 (s, 3H), 3.60-3.58 (m, 2H), 3.52-3.50 (m, 2H), 3.49 (s, 2H), 3.37 (s, 3H), 1.19 (s, 6H).
Workup
- additionwas added dropwise
- customThe reaction was quenched with sat. NH4Cl (aq.) (30 mL)
- extractionthe aqueous layer was extracted with DCM (2×50 mL)
- dry with materialthe combined organic layers were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- dissolutionThe crude oil was dissolved in EtOAc (125 mL)
- washwashed with water (3×40 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- distillationThe material was purified by vacuum distillation (68-69° C., 4.4 mbar)
Sources & evidence
- ORD record
- ord-6693ef062015431b9ce925b300861e04
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221756B2
Reaction notes
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