Conditions | Yield |
---|---|
With calcium hydroxide In 5,5-dimethyl-1,3-cyclohexadiene; decane at 220℃; for 1h; Solvent; Reagent/catalyst; Reflux; Large scale; | 99.2% |
With H2SO4/TiO2-La2O3-solid acid catalyst at 185 - 195℃; for 12h; | 88.6% |
at 200℃; anschl. auf 270grad; | |
at 200℃; dann auf 270grad im Druckrohr erhitzen; | |
With silicate-catalyst at 200 - 220℃; unter Entfernen des entstehenden Wassers; |
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 20℃; for 16h; Cooling with ice; | 70% |
benzoyl chloride
(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol
glyceryl tribenzoate
Conditions | Yield |
---|---|
at 200℃; |
Conditions | Yield |
---|---|
at 250℃; |
Conditions | Yield |
---|---|
at 200℃; | |
at 200℃; |
Conditions | Yield |
---|---|
at 200℃; bei der Einwirkung auf Kaliumbenzoat; |
Conditions | Yield |
---|---|
im geschlossenen Rohr; |
2-benzoyloxypropane-1,3-diol
benzoyl chloride
A
glyceryl tribenzoate
B
2,3-bis-benzoyloxy-propan-1-ol
C
benzoic acid 3-hexanoyloxy-2-hydroxypropyl ester
Conditions | Yield |
---|---|
With (S)-1-methyl-2-((morpholin-1-yl)methyl)pyrrolidine; (methylcyclopentadienyl)tin(II) chloride 1.) CH2Cl2, 0 deg C, 30 min, 2.) CH2Cl2, 5 min, 3.) CH2Cl2, 0 deg C, 1h,; Yield given. Multistep reaction. Yields of byproduct given; |
Conditions | Yield |
---|---|
at 180 - 200℃; | |
at 180 - 200℃; |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 48h; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrahydrofuran / 2 h 2: triethylamine / tetrahydrofuran / 48 h View Scheme |
Conditions | Yield |
---|---|
With Merrifield resin-supported N3=P(MeNCH2CH2)3N at 23 - 25℃; for 0.2h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
In hexane for 2h; Inert atmosphere; Schlenk technique; | 75% |
Conditions | Yield |
---|---|
With scandium tris(trifluoromethanesulfonate) at 150℃; for 24h; Sealed tube; | 75% |
ethanol
glyceryl tribenzoate
sodium ethanolate
benzoic acid ethyl ester
ethanol
glyceryl tribenzoate
A
2,3-bis-benzoyloxy-propan-1-ol
B
2-hydroxy-2-phenylacetophenone
ethanol
glyceryl tribenzoate
A
sodium benzoate
B
benzoic acid ethyl ester
C
glycerol
glyceryl tribenzoate
N-(2-hydroxyethyl)-benzamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Merrifield resin-supported N3=P(MeNCH2CH2)3N / 0.2 h / 23 - 25 °C / Inert atmosphere 2: Merrifield resin-supported N3=P(MeNCH2CH2)3N / tetrahydrofuran / 23 - 25 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
With tris(2,4-pentanedionato)ruthenium(III); hydrogen; bis(trifluoromethanesulfonyl)amide; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In tetrahydrofuran at 130℃; under 45004.5 Torr; for 18h; Autoclave; | 87 %Chromat. |
1. | orl-rat LD50:11,700 mg/kg | NPIRI* Raw Material Data Handbook, Vol.1: Organic Solvents, 1974. 2 (1975),59. |
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