2-heptylundecan-1-ol

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 14.6 g (0.095 mol) of phosphorus oxychloride in hexane, 51.4 g (0.190 mol) of 2-heptylundecyl alcohol, 19.2 g (0.190 mol) of triethylamine in hexane were added dropwise while maintaining the temperature at not higher than 0° C. After ripening the mixture at 25° C., a hydrochloric acid salt of triethylamine was removed by washing. The solvent was also removed to obtain 59.1 g (0.095 mol) of bis(2-heptylundecyl) phosphoric chloride (not less than 95% purity was confirmed by 31-NMR) at 25° C. a hydrochloric acid salt of triethylamine was removed by washing The solvent was also removed

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The same reaction as in Reference Example 1 was carried out under the same conditions except that the 5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol in Reference Example 1 was replaced by 2-heptylundecanol, whereupon 65 g (yield: 80%) of 2-heptylundecyl glycidyl ether was obtained. The same reaction as in Reference Example 1

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 14.6 g (0.095 mol) of phosphorus oxychloride in hexane, 51.4 g (0.190 mol) of 2-heptylundecyl alcohol, 19.2 g (0.190 mol) of triethylamine in hexane were added dropwise while maintaining the temperature at not higher than 0° C. After ripening the mixture at 25° C., a hydrochloric acid salt of triethylamine was removed by washing. The solvent was also removed to obtain 59.1 g (0.095 mol) of bis(2-heptylundecyl) phosphoric chloride (not less than 95% purity was confirmed by 31-NMR) at 25° C. a hydrochloric acid salt of triethylamine was removed by washing The solvent was also removed

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The same reaction as in Reference Example 1 was carried out under the same conditions except that the 5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol in Reference Example 1 was replaced by 2-heptylundecanol, whereupon 65 g (yield: 80%) of 2-heptylundecyl glycidyl ether was obtained. The same reaction as in Reference Example 1

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The same reaction as in Reference Example 1 was carried out under the same conditions except that the 5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol in Reference Example 1 was replaced by 2-heptylundecanol, whereupon 65 g (yield: 80%) of 2-heptylundecyl glycidyl ether was obtained. The same reaction as in Reference Example 1

Conditions: temp:0.00; pressure:0.00; stir:

Conditions: temp:-10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: With nitrogen substitution, 540 ml of toluene and 138.0 grams (0.9 moles) of phosphorus oxychloride were added and cooled to −10 degrees C. To this mixture, a solution of 243.5 grams (0.9 moles; 1.0 in molar ratio) of 2-heptylundecanol and 91.1 grams (0.9 moles) of triethylamine was dripped, and the mixture was reacted for 12 hours at 0 degrees C. The mixture was then heated to 25 degrees C., and a triethylamine hydrochloride was. removed by filtering to obtain 1003.9 grams of a toluene solution of (2-heptylundecyl)dichlorophosphate (34.7% in concentration). the mixture was reacted for 12 hours at 0 degrees C The mixture was then heated to 25 degrees C removed by filtering

Conditions: temp:-10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: With nitrogen substitution, 540 ml of toluene and 138.0 grams (0.9 moles) of phosphorus oxychloride were added and cooled to −10 degrees C. To this mixture, a solution of 243.5 grams (0.9 moles; 1.0 in molar ratio) of 2-heptylundecanol and 91.1 grams (0.9 moles) of triethylamine was dripped, and the mixture was reacted for 12 hours at 0 degrees C. The mixture was then heated to 25 degrees C., and a triethylamine hydrochloride was removed by filtering to obtain 1003.9 grams of a toluene solution of (2-heptylundecyl)dichlorophosphate (34.7% in concentration). the mixture was reacted for 12 hours at 0 degrees C The mixture was then heated to 25 degrees C , and a triethylamine hydrochloride was removed by filtering

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To 14.6 g (0.095 mol) of phosphorus oxychloride in hexane, 51.4 g (0.190 mol) of 2-heptylundecyl alcohol, 19.2 g (0.190 mol) of triethylamine in hexane were added dropwise while maintaining the temperature at not higher than 0° C. After ripening the mixture at 25° C., a hydrochloric acid salt of triethylamine was removed by washing. The solvent was also removed to obtain 59.1 g (0.095 mol) of bis(2-heptylundecyl) phosphoric chloride (not less than 95% purity was confirmed by 31-NMR) at 25° C. a hydrochloric acid salt of triethylamine was removed by washing The solvent was also removed

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The same reaction as in Reference Example 1 was carried out under the same conditions except that the 5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol in Reference Example 1 was replaced by 2-heptylundecanol, whereupon 65 g (yield: 80%) of 2-heptylundecyl glycidyl ether was obtained. The same reaction as in Reference Example 1