تفاعل #310027
ord-89026591fcf6482bb6c6673d3fa3fb22
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المعالجة
- 1أخرىTo a 2-liter round bottom flask equipped with a mechanical stirred, Dean Stark trap
- 2أخرىfitted with a condenser under an atmosphere of dry nitrogen
- 3درجة الحرارةThe reaction was then heated to 100° C. over 50 minutes
- 4درجة الحرارةheated to 200° C. for over 140 minutes
- 5درجة الحرارةheated to 280° C. over 1 hour
- 6workup.WAITheld at 280° C. for 8.5 hours
- 7درجة الحرارةcooled to 230° C.
- 8workup.WAITheld at 230° C. for approximately 14 hours
- 9درجة الحرارةThe reaction was then cooled to 150° C.
- 10ترشيحfiltered through a dry, hot (150° C.) 600 mL Buchner funnel
- 11workup.ADDITIONcontaining a filter bed of Celite
- 12درجة الحرارةmaintained between 110° C. and 120° C. with the aid of a vacuum
- 13أخرىto afford a product
الإجراء التجريبي
Branched pentadecylphenol calcium salt was prepared from the alkylation of phenol with a branched chain C14-C18 olefin derived primarily from propylene pentamer. To a 2-liter round bottom flask equipped with a mechanical stirred, Dean Stark trap fitted with a condenser under an atmosphere of dry nitrogen was charged with 705 gm (2.32 moles) of a C15 branched alkylphenol followed by 500 gm of Chevron RLOP 100N oil. This mixture was cooled to approximately 13° C. using an ice bath and then 48.8 gm (1.16 moles) of calcium hydride (98% obtained from Aldrich Chemical Company) was added in approximately 10 gram portions with stirring. The reaction was then heated to 100° C. over 50 minutes and then heated to 200° C. for over 140 minutes and held at 200° C. for approximately 18 hours and then heated to 280° C. over 1 hour and held at 280° C. for 8.5 hours and then cooled to 230° C. and held at 230° C. for approximately 14 hours. The reaction was then cooled to 150° C. and filtered through a dry, hot (150° C.) 600 mL Buchner funnel containing a filter bed of Celite and maintained between 110° C. and 120° C. with the aid of a vacuum to afford a product containing 3.51 wt % calcium.