Triphenylphosphine → HCID 11730000, compound

HRID 1841288Notes

Reaction equation

HRID 1841288 reaction equation
N(C(OCC)=O)=NC(OCC)=O.[OH:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH:21]([O:27][CH2:28][CH3:29])[C:22]([O:24][CH2:25][CH3:26])=[O:23])=[CH:16][CH:15]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH:49]1[C:62]2[CH:61]([CH2:63][CH2:64]O)[C:60]3[C:55](=[CH:56][CH:57]=[CH:58][CH:59]=3)[O:54][C:53]=2[CH:52]=[CH:51][CH:50]=1>C1COCC1>[CH2:28]([O:27][CH:21]([CH2:20][C:17]1[CH:16]=[CH:15][C:14]([O:13][CH2:64][CH2:63][CH:61]2[C:62]3[CH:49]=[CH:50][CH:51]=[CH:52][C:53]=3[O:54][C:55]3[C:60]2=[CH:59][CH:58]=[CH:57][CH:56]=3)=[CH:19][CH:18]=1)[C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH3:29]

Participants

6

Procedure

Diethyl azodicarboxylate (40% solution in toluene, 1.61 g, 9.3 mmol) was added dropwise, under argon, over 10 min to a solution of ethyl 3-(4-hydroxyphenyl)-2-ethoxypropionate (2.23 g, 9.3 mmol) and triphenylphosphine (2.43 g, 9.3 mmol) in THF (45 ml). The mixture was stirred for 15 min, then a solution of 2-(9H-xanthen-9-yl)ethanol (2.0 g, 9.3 mmol) in THF (10 ml) was added dropwise over 10 min. The resulting mixture was stirred at room temperature for 60 h. The solvent was evaporated, the residue stirred with benzene (20 ml) and the resulting crystalline solid filtered off. The filtrate was evaporated and the residue purified by column chromatography on silica gel (benzene eluent) to give the title compound as an oil: (1.9 g, 45.8%).

Workup

  1. stirringThe resulting mixture was stirred at room temperature for 60 h
  2. customThe solvent was evaporated
  3. stirringthe residue stirred with benzene (20 ml)
  4. filtrationthe resulting crystalline solid filtered off
  5. customThe filtrate was evaporated
  6. customthe residue purified by column chromatography on silica gel (benzene eluent)

Sources & evidence

ORD record
ord-db46680bc4cf4ac9bacd1a227c90cc01
Source dataset
uspto-grants-2004_01
Patent number
US06683111B2

Reaction notes

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