HCID 86736116, compound → HCID 131711103, compound

HRID 1448861Notes

Reaction equation

HRID 1448861 reaction equation
[N:1]([C@H:4]1[C:7](=[O:8])[NH:6][C@H:5]1[CH2:9][CH:10](OC)[O:11]C)=[N+:2]=[N-:3]>Cl.O1CCOCC1.O>[N:1]([C@H:4]1[C:7](=[O:8])[NH:6][C@H:5]1[CH2:9][CH:10]=[O:11])=[N+:2]=[N-:3]

Participants

5

Reactant 1

HCID 86736116HCID 86736116, compound

Product 1

HCID 131711103HCID 131711103, compound

Reagents, catalysts & solvents 3

HCID 313Hydrochloric AcidSolventHCID 962WaterSolventHCID 312751,4-DioxaneSolvent

Procedure

A mixture of 500 mg (2.5 mmole) of cis-3-azido-2-(2,2-dimethoxyethyl)-4-oxoazetidine in 10 ml of 5% HCl and 10 ml of dioxane was stirred at 35° for 1/2 hour. The mixture was diluted with water and extracted with 50 ml of benzene. The aqueous phase was saturated with brine and extracted 10 times with 50 ml of ethyl acetate. The ethyl acetate extract was dried over magnesium sulfate and evaporated to dryness. The residue was titurated with ether to give the desired aldehyde, 235 mg (60%), mp 73°-78°.

Workup

  1. extractionextracted with 50 ml of benzene
  2. extractionextracted 10 times with 50 ml of ethyl acetate
  3. extractionThe ethyl acetate extract
  4. dry with materialwas dried over magnesium sulfate
  5. customevaporated to dryness

Sources & evidence

ORD record
ord-fc67747ef7814b638bfec9010bb5de32
Source dataset
uspto-grants-1980_02
Patent number
US04187375

Reaction notes

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