Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | N,N-Diethylglycine | HCID 74151 | — |
Reaction Steps
Diethylamine (9.5 L) was charged into a 20 L glass-lined reactor and cooled to 3° C. Chloroacetic acid (1.21 kg) in MTBE (1.8 L) was added over 1 hour with cooling—the temperature rose to 16° C. during the addition. The mixture was warmed to 20° C., stirred over night and concentrated on rotary evaporator giving yellow oil. This oil was re-concentrated with iPrOAc, mixed with iPrOAc (4.5 L) and stirred over night. The off-white hygroscopic precipitate was filtered, washed with iPrOAc (1.5 L) and immediately placed into a drying cabinet to avoid deliquescence. After drying, titled product was obtained (820 g, Y=49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08227428B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-27b689454e0a40369c14617ecde24831 |
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| Source note | uspto-grants-2012_07 |
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