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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263378Generated: November 1, 2026

2-Thiophenecarboxaldehyde → HCID 69540551, compound

https://huagongshe.com/reaction/1263378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
Reactant5-Amino-2-methylphenolHCID 17818—
ReactantSodium AcetateHCID 517045—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 69540551HCID 6954055132.5%

Reaction Steps

To a solution of 5-amino-2-methylphenol (12.30 g, 100 mmole) in methanol (100 mL) at 4° C. was added 2-thiophenecarboxaldehyde (16.82 g, 150 mmole) and sodium acetate (16.41 g, 200 mmole). The reaction mixture was stirred for 15 minutes and sodium borohydride (4.73 g, 125 mmole) was added portionwise over 1 hour at 4° C. After the addition was complete, the reaction was allowed to stir for an additional 1.5 hours. The reaction mixture was poured onto crushed ice slurry (200 g) and the resulting precipitate was collected, washed with cold water three times and air-dried to afford 2-methyl-5-(thiophen-2-yl-methylamino)phenol (7.12 g, 32% yield): mp 130.8-132.6° C.; 1HNMR (400 MHz, DMSO-d6) δ 1.94 (s, 3H), 4.34 (d, 2H, J=6.0 Hz), 5.91 (t, 1H, J=6.1 Hz), 6.00 (dd, 1H, J=2.3, 8.0 Hz), 6.11 (d, 1H, J=2.2 Hz), 6.70 (d, 1H, J=8.1 Hz), 6.95 (dd, 1H, J=3.5, 5.0 Hz), 7.00 (dd, 1H, J=0.8, 3.4 Hz), 7.34 (dd, 1H, J=1.0, 5.0 Hz), 8.79 (s, 1H); MS m/z 219 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06540793B1
Source datasetuspto-grants-2003_04
ORD IDord-9bde9e01a4bf40ad94a7370e311e8468
Source noteuspto-grants-2003_04