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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263376Generated: October 31, 2026

Pyrrole-2-carboxaldehyde → HCID 11390060, compound

https://huagongshe.com/reaction/1263376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
Reactant5-Amino-2-methylphenolHCID 17818—
ReactantSodium AcetateHCID 517045—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 11390060HCID 1139006041%

Reaction Steps

To a stirred solution of 5-amino-2-methylphenol (9.84 g, 80 mmole) in methanol (100 mL) at 4° C. was added pyrrole-2-carboxaldehyde (11.41 g, 120 mmole) and sodium acetate (13.13 g, 160 mmole). The reaction mixture was stirred for 15 minutes and sodium borohydride (3.78 g, 100 mmole) was added portionwise over 1 hour at 4° C. After the addition was complete, the reaction was allowed to stir for an additional 3 hours. The reaction mixture was poured onto crushed ice slurry (200 g) and the resulting precipitate was collected and washed with cold water three times and air-dried to afford 2-methyl-5-[(1H-pyrrol-2-yl-methyl)amino]phenol (6.62 g, 41% yield): mp 115.4-116.8° C.; 1HNMR (400 MHz, DMSO-d6) δ 1.94 (s, 3H), 4.03 (d, 2H, J=5.6 Hz), 5.37 (t, 1H, J=5.6 Hz), 5.90 (m, 2H), 6.01 (dd, 1H, J=2.2, 8.0 Hz), 6.12 (d, 1H, J=2.1 Hz), 6.61 (m, 1H), 6.70 (d, 1H, J=8.1 Hz), 8.77 (s, 1H), 10.64 (s, 1H); MS m/z 202 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06540793B1
Source datasetuspto-grants-2003_04
ORD IDord-c2b90314c2154634a66c7fbad5a7c73e
Source noteuspto-grants-2003_04