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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560556Generated: October 29, 2026

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

https://huagongshe.com/reaction/560556

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 numberUS08063084B2
Source datasetuspto-grants-2011_11
ORD IDord-b8f7234f0464487caaedf37cbaf0ee88
Source noteuspto-grants-2011_11