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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067329Generated: November 4, 2026

Hydrazine hydrate (1:1) → Ethyl 5-(hydrazinecarboxamido)-3-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/2067329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantEthyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylateHCID 43403943—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(hydrazinecarboxamido)-3-methylthiophene-2-carboxylateHCID 6663191489%

Reaction Steps

To a stirred suspension of ethyl 3-methyl-5-(phenoxycarbonylamino)-thiophene-2-carboxylate (18.89 g, 61.86 mmol) in tetrahydrofuran (130 mL) was added hydrazine monohydrate (19.0 mL, 391.7 mmol). The resulting reaction mixture was stirred for 2.5 h, and then concentrated in vacuo. The residue was triturated with ethyl acetate to afford ethyl 5-(hydrazinecarboxamido)-3-methylthiophene-2-carboxylate as a yellowish solid in 89% yield (13.30 g): MS (ES+) m/z 244.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293768B2
Source datasetuspto-grants-2012_10
ORD IDord-d0f4d7d2d41040859ee0ead76e57f82e
Source noteuspto-grants-2012_10