| Identification | More | [Name]
2',5'-DIHYDROXYPROPIOPHENONE | [CAS]
938-46-5 | [Synonyms]
1-(2,5-DIHYDROXYPHENYL)PROPAN-1-ONE
2',5'-DIHYDROXYPROPIOPHENONE
2,5-DIHYDROXYPROPIOPHENONE
2-PROPIONYLHYDROQUINONE
1-(2,5-Dihydroxyphenyl)-1-propanone
1-Propanone, 1-(2,5-dihydroxyphenyl)-
2’,5’-dihydroxy-propiophenon
Propiophenone, 2',5'-dihydroxy- | [EINECS(EC#)]
213-343-8 | [Molecular Formula]
C9H10O3 | [MDL Number]
MFCD00016465 | [Molecular Weight]
166.17 | [MOL File]
938-46-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RTECS ]
UH0420000 |
| Hazard Information | Back Directory | [Chemical Properties]
yellowish crystalline powder | [Preparation]
Preparation by Fries rearrangement of quinol dipropionate (hydroquinone dipropionate),
with aluminium chloride without solvent at 130–140° for 4 h (75%), ? at 142° for 30 min (80%), at 160–165° for 3 h (good yields) or at 190–200° for 90 min (60%)
by using various quantities of aluminium chloride at 180° for 2 h (to see ? below)
with aluminium chloride (2 equiv) in nitromethane at 20° for a week (7%) ? or in nitrobenzene (24%)
with boron trifluoride complex (BF? 3-OBu2) at reflux for 1 h (42%)
by using titanium tetrachloride (2 equiv) at 130° for 2 h gave only 6% yield
Also obtained by treatment of
hydroquinone dipropionate with aluminium chloride in the presence of hyd-? roquinone (61%)
2-hydroxy-5-(propionyloxy)propiophenone with aluminium chloride (5 equiv) ? at 180° for 30 min in the presence of hydroquinone (57%)
Also obtained by acylation of hydroquinone with propionic acid
in the presence of boron trifluoride in ethylene dichloride at 50–55° (59%) ?, in tetrachloroethane at 90–95° for 5 h (70%) or at 50° for 4 h (70%) or without solvent (67%) at 80° for 2 h (54%) or at 125° for 2 h (71%)
in the presence of zinc chloride at 190° few min (Nencki reaction)
in the presence of 70% perchloric acid at reflux for 1 h (12%)
Also obtained by Friedel–Crafts acylation of hydroquinone with propionyl chlo-ride in nitrobenzene in the presence of aluminium chloride (40%)
Also obtained from 2-hydroxy-5-(propionyloxy)propiophenone; the ester group elimination on hydrolysis with 85% sulfuric acid at r.t. or by treatment with by aluminium chloride
Also obtained by reaction of benzoquinone (2.5 equiv) with 2-oxobutanoic acid in aqueous acetonitrile or an acetonitrile/methylene chloride mixture (91%). |
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