HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-2-tert-Butoxycarbonylamino-5-oxo-hexanoic acid ethyl ester → (S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-2-tert-Butoxycarbonylamino-5-oxo-hexanoic acid ethyl ester | HCID 58544329 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | (S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156823B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-6be19fac10084c26b3be6b861f3064eb |
| Source note | uspto-grants-2015_10 |