Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 69691057 | HCID 69691057 | 88% |
Reaction Steps
To a solution of 15.00 g (122 mmol) of p-anisidine in 100 mL of DMF under N2 was added 23.50 g (141 mmol) of ethyl bromoacetate and 14.95 g (141 mmol) anhydrous sodium carbonate. The mixture was heated to 70° C. for 16 hours and then cooled to room temperature. Water (500 mL) was added and the mixture stirred vigorously until a precipitate formed. The solid was collected and washed with 100 mL water, then dried in vacuo to give 19.59 g (88%) of the desired compound as a grey solid. 1H NMR (CDCl3): δ 6.81 (d, J=8.8, 2H); 6.579 (d, J=8.8, 2H); 4.24 (q, J=7.0, 2H); 4.10 (s, 1H); 3.86 (s, 2H); 3.75 (s, 3H); 1.28 (t, J=7.0, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602895B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-ac03dd621a0a4ac7b7daf9b81cd1d111 |
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| Source note | uspto-grants-2003_08 |
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