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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39654Generated: October 26, 2026

Iodine → 2-(N'-benzyloxycarbonyl-hydrazino)-2-methyl-propionic acid ethyl ester

https://huagongshe.com/reaction/39654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPyridineHCID 1049—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantBenzyl carbazateHCID 79242—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(N'-benzyloxycarbonyl-hydrazino)-2-methyl-propionic acid ethyl esterHCID 15282579—

Reaction Conditions

Temperature97.5 °C

Reaction Steps

Benzyl carbazate (25 g, 0.15 mol) was dissolved in 50 mL of DMF in a round bottom flask. The solution was heated to 95-100° C. From two separate addition funnels, ethyl 2-bromoisobutyrate (58.5 g, 0.3 mol) and pyridine (29.7 g, 0.375 mol, 30 mL) were added drop-wise separately and simultaneously over 30-120 minutes. Heating was continued if necessary to propel the reaction to completion. The reaction was monitored by TLC (30% ethyl acetate in hexanes, I2 visualization). The mixture was allowed to cool, and then poured onto ice water. The aqueous mixture was extracted with ethyl ether, and the solvent was removed in vacuo. 2-(N′-benzyloxycarbonyl-hydrazino)-2-methyl-propionic acid ethyl ester was isolated, optionally after silica gel chromatography. 1H NMR (300 MHz, CDCl3) δ (ppm): 7.36 (br s, 5H), 6.6 (br s, 1H), 5.15 (br s, 2H), 4.2 (q, 2H), 1.3 (s, 6H), 1.25 (t, 3H). 1H NMR analysis alone is insufficient to ascertain the extent of the reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524948B2
Source datasetuspto-grants-2013_09
ORD IDord-dd0158b28910400fb2c1313ddaee24f1
Source noteuspto-grants-2013_09