Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353835Generated: November 1, 2026

Formamide → HCID 17990151, compound

https://huagongshe.com/reaction/2353835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantAmmonium formateHCID 2723923—
ReactantEthyl 2-amino-4,7-dihydro-5H-spiro[1-benzothiophere-6,2'-[1,3]dioxolane]-3-carboxylateHCID 10902110—
ProductHCID 17990151HCID 1799015188%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a stirring solution of ethyl 2-amino-4,7-dihydro-5H-spiro[1-benzothiophene-6,2′-[1,3]dioxolane]-3-carboxylate (40.0 g, 0.142 mol) in formamide (225 mL) was added ammonium formate (17.8 g, 0.282 mol). The resulting mixture was stirred with at 140° C. for 16 h, after which time the heterogeneous contents were removed from heating, and allowed to cool to rt. The contents were filtered, the solid filter cake was washed with water (2×60 mL), and suction dried overnight to afford the desired product as an off-white solid (33.0 g, 88%). 1H-NMR (DMSO-d6) δ 12.35 (broad s, 1H), 8.00 (s, 1H), 3.92 (s, 4H), 2.95 (t, 2H), 2.91 (s, 2H), 1.83 (t, 2H); LCMS RT=1.87 min, [M+H]+=265.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750017B2
Source datasetuspto-grants-2010_07
ORD IDord-51b85c54723244e3ae6b2912d8c17bd6
Source noteuspto-grants-2010_07