Tetrahydrofuran → 5-(2-tert-butoxycarbonyl-vinyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester
Reaction equation
[CH3:1][C:2]([CH3:5])([O-:4])[CH3:3].[Na+].[Br-].C1([PH+](C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:27]([O:29][C:30]([C:32]1[NH:33][C:34]([CH:38]=O)=[CH:35][C:36]=1[CH3:37])=[O:31])[CH3:28].C1C[O:43][CH2:42][CH2:41]1>>[CH2:27]([O:29][C:30]([C:32]1[NH:33][C:34]([CH:38]=[CH:41][C:42]([O:4][C:2]([CH3:5])([CH3:3])[CH3:1])=[O:43])=[CH:35][C:36]=1[CH3:37])=[O:31])[CH3:28]Participants
Procedure
Sodium tert-butoxide (1.37 g, 14.3 mmol) was added to the dry tert-butoxycarbonylmethyl)triphenylphosphonium bromide (6.56 g, 14.3 mmol) in THF (anhydrous, 30 mL) under nitrogen. The mixture was stirred at room temperature for 30 minutes. To the mixture was added 5-formyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (2.36 g, 13 mmol) in THF (35 mL). The mixture was then stirred at room temperature under nitrogen for overnight. The solid was filtered off and the filtrate was concentrated followed by column chromatograph (10% EtOAc in hexane) to give 2.95 g (81%) of 5-(2-tert-butoxycarbonyl-vinyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester. 1H NMR (300 MHz, DMSO-d6) δ 11.85 (br s, 1H, NH), 7.35 (d, J=15.7 Hz, 1H), 6.73 (s, 1H), 6.41 (d, J=15.7 Hz, 1H), 4.23 (q, J=7.1 Hz, 2H, OCH2), 2.22 (s, 3H, CH3), 1.44 (s, 9H, 3×CH3), 1.28 (t, J=7.1 Hz, 3H, OCH2CH3). MS 279 [M+].
Workup
- stirringThe mixture was then stirred at room temperature under nitrogen for overnight
- filtrationThe solid was filtered off
- concentrationthe filtrate was concentrated
Sources & evidence
- ORD record
- ord-0e731b7f3dcc4a76995db5444505a729
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06908930B2
Reaction notes
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