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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737851Generated: November 4, 2026

Ammonium Chloride → tert-Butyl (S)-5-amino-3,4-dihydro-2H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1737851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl (S)-5-(methylsulfanyl)-3,4-dihydro-2H-pyrrole-2-carboxylateHCID 53965507—
SolventMethanolHCID 887—
Producttert-Butyl (S)-5-amino-3,4-dihydro-2H-pyrrole-2-carboxylateHCID 53795147—

Reaction Steps

To a solution of (S)-2-methylsulfanyl-3,4-dihydro-5H-pyrrole-5-carboxylic acid t-butyl ester (0.42 g, 1.95 mmol) in 4.0 mL anhydrous MeOH was added anh NH4Cl (0.11 g, 2.05 mmol). The reaction mixture was heated to reflux for 2 h, concentrated in vacuo, and the residue was taken up in CH2C2. The white solids were filtered, and the filtrate was concentrated to provide (S)-2-amino-3,4-dihydro-5H-pyrrole-5carboxylic acid t-butyl ester.HCl (0.41 g, 94%) as a light yellow solid 1H NMR (CDCl3) δ 1.49 (s, 9H), 2.24 (m, 1H), 2.52 (m, 1H), 3.06-3.08 (m, 2H), 4.44 (m, 1H), 9.81-9.8 (m, 2H). MS calcd for C9H16N2O2 +H 185, found 185.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962487
Source datasetuspto-grants-1999_10
ORD IDord-6af4239c47d8489887b4e1512427ce1c
Source noteuspto-grants-1999_10