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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445339Generated: October 31, 2026

Benzylamine → N-benzyl-3-hydroxythiophene-2-carboxamide

https://huagongshe.com/reaction/1445339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Hydroxythiophene-2-carboxylic acidHCID 54715543—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-3-hydroxythiophene-2-carboxamideHCID 54704139—

Reaction Conditions

Temperature22 °C

Reaction Steps

1.44 g of 3-hydroxy-thiophene-2-carboxylic acid were dissolved in 100 ml of dichloromethane, and 2.18 ml of benzylamine and 5.00 ml of a 50% strength 1-propanephosphoric anhydride solution in acetic acid were added. The reaction mixture was stirred at 22° C. for 2 h and, after addition of 100 ml of saturated sodium bicarbonate solution, extracted twice with 100 ml of dichloromethane each time. The combined organic phases were washed with 100 ml of saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The product with the molecular weight of 233.3 (C12H11NO2S), MS (ESI): 234 (M+h+) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666848B2
Source datasetuspto-grants-2010_02
ORD IDord-3e2dc9052fd44cb1968b0c0906117366
Source noteuspto-grants-2010_02