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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509697Generated: October 31, 2026

(S)-2-tert-Butoxycarbonylamino-5-oxo-hexanoic acid ethyl ester → (S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1509697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-tert-Butoxycarbonylamino-5-oxo-hexanoic acid ethyl esterHCID 58544329—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product(S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylateHCID 67682752—

Reaction Steps

(S)-ethyl 2-(tert-butoxycarbonylamino)-5-oxohexanoate in a 1 L flask was treated with a trifluoro acetic acid/dichloromethane solution (1:1 mixture, 100 mL). Effervescence was observed and the mixture was allowed to stir for 4 hours at room temperature. After which time the volatiles were removed in vacuo to yield (S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate as an oil, and used directly in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221833B2
Source datasetuspto-grants-2015_12
ORD IDord-4dfb38d4da7e4dde87b65d044e33b0b9
Source noteuspto-grants-2015_12