HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992213Generated: October 29, 2026
Triethylamine → Methyl 2,2-dimethyl-3-[(methylsulfonyl)amino]propanoate
https://huagongshe.com/reaction/1992213
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 3-amino-2,2-dimethylpropanoate | HCID 13285789 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2,2-dimethyl-3-[(methylsulfonyl)amino]propanoate | HCID 86608479 | 31.2% |
Reaction Steps
To a solution of methyl 3-amino-2,2-dimethylpropanoate (249 mg, 1.90 mmol) and Et3N (0.80 mL, 5.70 mmol) in 2 mL CH2Cl2 was added methanesulfonyl chloride (0.29 mL, 3.80 mmol). The reaction was stirred for 2 days, quenched by the addition of saturated aqueous NaHCO3, extracted with CHCl3, and chromatographed (1:1 hex:EtOAc) to provide methyl 2,2-dimethyl-3-[(methylsulfonyl)amino]propanoate (124 mg, 31%) as a clear oil. 1H NMR (400 MHz, CDCl3), 4.95 (t, 1H, J=6.8 Hz), 3.69 (s, 3H), 3.16 (d, 2H, J=6.8 Hz), 2.95 (s, 3H), 1.24 (s, 6H). Methyl 2,2-dimethyl-3-[(methylsulfonyl)amino]propanoate was hydrolyzed using aqueous NaOH to provide 2,2-dimethyl-3-[(methylsulfonyl)amino]propanoic acid, which was used without further purification. 1H NMR (400 MHz, CDCl3), δ 10.28 (br. s, 1H), 5.56 (br. s, 1H), 3.14 (s, 2H), 2.94 (s, 3H), 1.25 (5, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645771B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-52b5b79f32be45c18dd34fa45ad39be5 |
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| Source note | uspto-grants-2010_01 |
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