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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916356Generated: October 31, 2026

Methanol--water (1/1) → Methyl 3-amino-5-bromothiophene-2-carboxylate

https://huagongshe.com/reaction/1916356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanol--water (1/1)HCID 22242641—
ReactantMethyl 5-bromo-3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 56965789—
SolventPotassium CarbonateHCID 11430—
ProductMethyl 3-amino-5-bromothiophene-2-carboxylateHCID 20158931100%

Reaction Steps

Methyl 5-bromo-3-(trifluoroacetylamino)-2-thiophenecarboxylate (2.0 g, 6.2 mmol) was stirred in 120 mL of 0.25 N K2CO3 in 7:3 MeOH/water. After 2.5 h, the bulk of the MeOH was removed in vacuo. The residue was partitioned between brine (75 mL) and CH2Cl2 (100 mL). The organic layer was dried (MgSO4) and concentrated in vacuo to provide methyl 5-bromo-3-amino-2-thiophenecarboxylate as a yellow solid (1.4 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618115B2
Source datasetuspto-grants-2013_12
ORD IDord-35954111250448da81286aa2ce179c1a
Source noteuspto-grants-2013_12