Production Method 1

4475-96-1

93169-29-0

Reaction Conditions

1.1 Reagents: 2-Mercaptoethanol ,  Hydrochloric acid Solvents: Tetrahydrofuran

Reference

Conversion of α-amino nitriles to amides by a new Pinner-type reaction

Lee, Young Bok; Goo, Yang Mo; Lee, Youn Young; Lee, Jae Keun, Tetrahedron Letters, 1990, 31(8), 1169-70

Production Method 2

4475-96-1

93169-29-0

Reaction Conditions

1.1 Reagents: 2-Mercaptoethanol Solvents: Water

Reference

Hydrolysis of various nitrile compounds to the amides by catalysis of 2-mercaptoethanol in a phosphate buffer

Lee, Young Bok; Goo, Yang Mo; Lee, Youn Young; Lee, Jae Keun, Tetrahedron Letters, 1989, 30(52), 7439-40

Production Method 3

88463-19-8

93169-29-0

Reaction Conditions

1.1 Reagents: Hydrogen ,  Hydrochloric acid Solvents: Water

Reference

Stereochemical preference in the reactions of N-protected L-amino acid 1-hydroxybenzotriazole esters with racemic amino acid derivatives

Miyazawa, Toshifumi; Ozawa, Ayako; Furuhashi, Motohiro; Munegumi, Toratane, Protein & Peptide Letters, 2009, 16(3), 297-300

Production Method 4

93169-29-0

Reaction Conditions

Reference

Base-catalyzed racemization of α-amino acid amides

, Japan, , ,

Production Method 5

93169-29-0

Reaction Conditions

Reference

Racemizing an optically active N-benzylidene amino acid amide

, European Patent Organization, , ,

2-Amino-3-methylbutanamide Hydrochloride Raw materials

• Carbamic acid, [1-(aminocarbonyl)-2-methylpropyl]-, phenylmethyl ester
• 2-amino-3-methylbutanenitrile

2-Amino-3-methylbutanamide Hydrochloride Preparation Products

• 2-Amino-3-methylbutanamide Hydrochloride (93169-29-0)

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