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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | (S)-N'-(2-(Benzyloxy)propylidene)formohydrazide | HCID 54011714 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-((1S,2S)-1-Ethyl-2-(phenylmethoxy)propyl)hydrazinecarboxaldehyde | HCID 10130911 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102664B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-eebf30ad9c17471089b6353d67ad7c70 |
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| Source note | uspto-grants-2015_08 |
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