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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368076Generated: October 29, 2026

Nitromethane → HCID 69688505, compound

https://huagongshe.com/reaction/1368076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
ReactantHCID 69688152HCID 69688152—
ProductHCID 69688505HCID 6968850596.1%

Reaction Steps

Ethyl 4-(S)-benzyloxycarbonylamino-4-cyclopropyl-2-butenoate was dissolved in dry nitromethane (15 ml), and the solution was mixed with 1,1,3,3-tetramethylguanidine (133 μl, 1.05 mol) and stirred at room temperature for 17 hours. The reaction solution was concentrated under a reduced pressure, the resulting residue was dissolved in chloroform (50 ml), and the solution was washed with 10% citric acid aqueous solution (50 ml) and saturated sodium chloride aqueous solution (50 ml) in that order, and then dried over anhydrous magnesium sulfate, thereby obtaining 1.207 g (96.1%) of the title compound as a yellow oil. This product (diastereomer mixture) was used in the subsequent reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573260B1
Source datasetuspto-grants-2003_06
ORD IDord-48e1186bf58d4fae8ecc7b4d4f1d012d
Source noteuspto-grants-2003_06