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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512814Generated: October 31, 2026

Iodine → 2-((1S,2S)-1-Ethyl-2-(phenylmethoxy)propyl)hydrazinecarboxaldehyde

https://huagongshe.com/reaction/512814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl BromideHCID 6332—
Reactant(S)-N'-(2-(Benzyloxy)propylidene)formohydrazideHCID 54011714—
Solventtert-Butyl methyl etherHCID 15413—
Product2-((1S,2S)-1-Ethyl-2-(phenylmethoxy)propyl)hydrazinecarboxaldehydeHCID 10130911—

Reaction Conditions

Temperature42.5 °C

Reaction Steps

A mixture of methyl tertiary butyl ether (150 ml), Mg turnings (18 g) and I2 (0.03 g) was heated to 40-45° C. under nitrogen atmosphere and ethyl bromide (81.8 g) was added slowly to the reaction mixture for about 1 hour. The reaction mixture was further heated to 50-55° C. and methyl tertiary butyl ether (60 ml) was added to it. The reaction mixture was stirred for 2 hours at 50-55° C. and cooled 0-10° C. N,O-Bistrimethyl silyl acetamide (60.9 g) was added to a mixture of methyl tertiary butyl ether (150 ml) and (S)—N′-(2-(benzyloxy)propylidene)formohydrazide compound of formula-16 (30 g) over a period of 45 minutes at 25-30° C. and stirred for 1 hour at 25-30° C. This reaction mixture was added to the above reaction mixture at 0-10° C. under nitrogen atmosphere. Temperature of the reaction mixture was raised to 25-30 C and stirred for 8 hours at 25-30° C. After completion of reaction, the reaction mixture was quenched with 8% acetic acid in chilled water. The reaction mixture was stirred for 30 minutes at 25-30° C. and both organic and aqueous layers were separated. The organic layer was washed with 10% sodium chloride solution and followed by water. Distilled off the solvent completely to get the title compound. The obtained compound was taken into next step without isolating the compound. Yield: 48 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102664B2
Source datasetuspto-grants-2015_08
ORD IDord-eebf30ad9c17471089b6353d67ad7c70
Source noteuspto-grants-2015_08