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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575636Generated: October 25, 2026

Ethyl formate → HCID 178503475, compound

https://huagongshe.com/reaction/575636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantBis(S-methylisothiouronium) sulfateHCID 13347—
ReactantSodium hydrideHCID 24758—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 2-(cyclopropylmethoxy)acetateHCID 43119684—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178503475HCID 17850347517.7%

Reaction Steps

To a stirred suspension of NaH (35.20 g, 0.88 mol, 60% in mineral oil) in anhydrous THF (1000 mL) was added ethyl formate (88.80 g, 0.90 mol) and the title compound of step 1 (126.0 g, 0.80 mol) in anhydrous THF (100 mL). The mixture was stirred at r.t. for 0.5 hour and refluxed for 3 h. In a separate flask, S-methylthiopseudourea hemisulfate (133.44 g, 0.96 mol) and sodium ethoxide (65.28 g, 0.96 mol) in EtOH (200 mL) were stirred at r.t. for 1 h, whereupon this mixture was added to the above mixture. There combined mixture was refluxed for 15 h, cooled, and the pHwas adjusted to 5 with acetic acid. After concentration under vacuum, silica gel chromatography (DCM: MeOH=50/110/1) gave the title compound (30.00 g, 17.7% yield) as a yellow solid. 1H NMR (CDCl3, 400 MHz) δ 12.08 (s, 1H), 7.49 (s, 1H), 3.83-3.80 (m, 2H), 2.55 (s, 3H), 1.37-1.28 (m, 1H), 0.65-0.62 (m, 2H), 0.37-0.34 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-726dad1c58e74da3ba4ad617c1fe9dc4
Source noteuspto-grants-2015_05