Hydrochloric Acid → 3-Amino-2,2-dimethyl-propionic acid TFA salt

HRID 1481150ノート

反応式

HRID 1481150 の反応式
C[O:2][C:3](=[O:16])[C:4]([CH3:15])([CH3:14])[CH2:5][NH:6]C(OC(C)(C)C)=O.[OH-].[Na+].Cl.[C:20]([OH:26])([C:22]([F:25])([F:24])[F:23])=[O:21]>CO.C(Cl)Cl>[OH:26][C:20]([C:22]([F:25])([F:24])[F:23])=[O:21].[NH2:6][CH2:5][C:4]([CH3:15])([CH3:14])[C:3]([OH:16])=[O:2]

参加物

7

実験手順

To a solution of 3-tert-butoxycarbonylamino-2,2-dimethyl-propionic acid methyl ester (2.5 g, 10.8 mmol) in MeOH (30 mL) was added 1 M NaOH (27 mL, 27 mmol), and the resulting mixture was stirred at r.t. for 16 h. 1 M HCl was added until pH was ˜3, and the mixture was extracted with EtOAc. The organic layer was dried over MgSO4 and concentrated. The residue obtained was dissolved CH2Cl2 (10 mL), and TFA (7 mL) was added. The resulting mixture was stirred at r.t. for 3 days, then concentrated to dryness to give 2.1 g of the title compound as a gray solid. 1H NMR (DMSO-d6, 200 MHz): δ ppm=7.8 (br s, 3H), 2.80-3.00 (m, 2H), 1.18 (s, 6H).

後処理

  1. extractionthe mixture was extracted with EtOAc
  2. dry with materialThe organic layer was dried over MgSO4
  3. concentrationconcentrated
  4. customThe residue obtained
  5. additionwas added
  6. stirringThe resulting mixture was stirred at r.t. for 3 days
  7. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-fa98b959a7ec4d7fad1f4089dcda8fb0
出典データセット
uspto-grants-2016_08
特許番号
US09409892B2

反応ノート

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