반응 #449137

반응 방정식

oxalyl chloride

allyl alcohol

allyl alcohol

3-t-butylperoxy-1,3-dimethylbutanol

→

Allyl 3-t-Butylperoxy-1,3-dimethylbutyl Oxalate

용매

ethyl acetate

반응 조건

후처리

1. 1
   기타A second preparation of I-4
2. 2
   기타A 100 mL 3-necked flask equipped with a magnetic stirring bar, a nitrogen inlet line
3. 3
   기타was bubbled through the oxalyl chloride
4. 4
   기타remained below 15° C
5. 5
   workup.ADDITIONThe addition
6. 6
   workup.ADDITIONwas added
7. 7
   기타The contents were then transferred to a one-necked flask
8. 8
   기타the solvent and excess oxalyl chloride were then removed
9. 9
   기타a rotary evaporator
10. 10
    기타Obtained
11. 11
    온도The oil was cooled to 10° C. and to it
12. 12
    기타was stripped on a rotary evaporator
13. 13
    기타Obtained

실험 절차

A second preparation of I-4 was carried out. A 100 mL 3-necked flask equipped with a magnetic stirring bar, a nitrogen inlet line, a thermometer and an addition funnel with a side arm was charged with 25.9 g(200 mmoles) of oxalyl chloride, dry nitrogen gas was bubbled through the oxalyl chloride and the flask contents were cooled to 0° C. Then 20.0 g (97.3 mmoles) of 92.6% 3-t-butylperoxy-1,3-dimethylbutanol was added dropwise at such a rate that the temperature remained below 15° C. The addition took 30 minutes to complete. The reaction mass was then stirred for 60 minutes at 15° C. after which 50 mL of dry ethyl acetate was added. The contents were then transferred to a one-necked flask and the solvent and excess oxalyl chloride were then removed using a rotary evaporator. Obtained was 29.3 g of a light yellow oil. The oil was cooled to 10° C. and to it was added 6.0 g (103.3 mmoles) of allyl alcohol over a period of 15 minutes while a vigorous stream of dry nitrogen was swept through the reaction mass. The temperature was held below 20° C. during the addition of allyl alcohol. The reaction mixture was then stirred for 60 minutes at 15°-20° C. after which it was stripped on a rotary evaporator. Obtained was 31.7 g (>100% of theory, uncorrected) of a light yellow liquid. GC showed a single large peak, 93% by area. An IR spectrum of the product showed carbonyl bands at 1770 cm-1 and 1750 cm-1 and a peroxide (--OO--) band at 875 cm-1.

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