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5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE synthesis

3synthesis methods
(2S)-5-Allyl-1,2-pyrrolidinedicarboxylic acid 1-(tert-butyl) 2-methyl ester

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5-ETHENYL-L-PROLINE METHYL ESTER HYDROCHLORIDE

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-

Yield:-

Steps:

Multi-step reaction with 4 steps
1: 1.) O3; 2.) NaBH4 / 1.) MeOH, CH2Cl2, -78 deg C; 2.) MeOH, CH2Cl2, -78 deg C to RT
2: (n-Bu)3P / tetrahydrofuran
3: 1.) MCPBA; 2.) Me2S, Et3N / 1.) CH2Cl2, -70 deg C, 30 min; 2.) CH2Cl2, -70 deg C to RT
4: TFA / CH2Cl2

References:

Beal, Laura M.;Moeller, Kevin D. [Tetrahedron Letters,1998,vol. 39,# 26,p. 4639 - 4642]