Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86134692 | HCID 86134692 | 100% |
Reaction Steps
Ethyl 2-bromoacetate (146 mL, 1.3 mol) was added dropwise to a stirred solution of 4-methoxyaniline (3) (75 g, 0.61 mol) and DIPEA (265 mL, 1.5 mol) in MeCN (300 mL). The reaction mixture was stirred at 60° C. for 16 h and then partitioned between 2 M HCl (aq.) (500 mL), and EtOAc (300 mL), the aqueous phase was extracted with EtOAc (300 mL) and the combined organics were washed succesively with 2 M HCl (aq.) (2×300 mL), water (500 mL), and brine (500 mL), dried (MgSO4), filtered and solvents removed in vacuo to give diethyl 2,2′-((4-methoxyphenyl)azanediyl)diacetate (4) (180 g, 100%) as a purple oil: m/z 296 (M+H)+ (ES+). 1H NMR (400 MHz, CDCl3) δ 6.82-6.78 (m, 2H), 6.64-6.59 (m, 2H), 4.19 (q, J=7.1 Hz, 4H), 4.10 (s, 4H), 3.74 (s, 3H), 1.27 (t, J=7.1 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221756B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-c668d14c98ee4827ac19b998255876a5 |
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| Source note | uspto-grants-2015_12 |
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