but-3-ynyl 4-chlorobenzenesulfonate

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

Conditions: temp:2.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A solution of 3-butyn-1-ol (365 g, 5.21 mol), triethylamine (526 g, 5.21 mol), and toluene (419 mL) was added to a cooled (0-5° C.) stirred solution of 4-chlorobenzenesulfonyl chloride (1.0 kg, 4.74 mol) and toluene (2.10 L). The reaction temperature was maintained below 20° C. during the addition. Precipitation of triethylamine hydrochloride salt occurred during the reaction. The reaction mixture was stirred at room temperature for 2-4 h. The triethylamine hydrochloride byproduct was separated by filtration and washed with toluene (2×350 mL). The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid. 2-Propanol (1.20 L) was added to the residue and the stirred solution was cooled to 20-25° C. Water (1.80 L) was added over 15 m. The slurry of product and solvent was cooled to 0-5° C. and stirred for 1 h. The white solid product was collected by filtration, washed with 33% aqueous 2-propanol (v/v), and vacuum dried to give 4-chloro-benzenesulfonic acid but-3-ynyl ester with 99% purity (as determined by HPLC. The reaction temperature was maintained below 20° C. during the addition Precipitation of triethylamine hydrochloride salt occurred during the reaction The triethylamine hydrochloride byproduct was separated by filtration washed with toluene (2×350 mL) The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid 2-Propanol (1.20 L) was added to the residue the stirred solution was cooled to 20-25° C Water (1.80 L) was added over 15 m The slurry of product and solvent was cooled to 0-5° C. stirred for 1 h The white solid product was collected by filtration washed with 33% aqueous 2-propanol (v/v), and vacuum dried

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

Conditions: temp:2.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A solution of 3-butyn-1-ol (365 g, 5.21 mol), triethylamine (526 g, 5.21 mol), and toluene (419 mL) was added to a cooled (0-5° C.) stirred solution of 4-chlorobenzenesulfonyl chloride (1.0 kg, 4.74 mol) and toluene (2.10 L). The reaction temperature was maintained below 20° C. during the addition. Precipitation of triethylamine hydrochloride salt occurred during the reaction. The reaction mixture was stirred at room temperature for 2-4 h. The triethylamine hydrochloride byproduct was separated by filtration and washed with toluene (2×350 mL). The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid. 2-Propanol (1.20 L) was added to the residue and the stirred solution was cooled to 20-25° C. Water (1.80 L) was added over 15 m. The slurry of product and solvent was cooled to 0-5° C. and stirred for 1 h. The white solid product was collected by filtration, washed with 33% aqueous 2-propanol (v/v), and vacuum dried to give 4-chloro-benzenesulfonic acid but-3-ynyl ester with 99% purity (as determined by HPLC. The reaction temperature was maintained below 20° C. during the addition Precipitation of triethylamine hydrochloride salt occurred during the reaction The triethylamine hydrochloride byproduct was separated by filtration washed with toluene (2×350 mL) The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid 2-Propanol (1.20 L) was added to the residue the stirred solution was cooled to 20-25° C Water (1.80 L) was added over 15 m The slurry of product and solvent was cooled to 0-5° C. stirred for 1 h The white solid product was collected by filtration washed with 33% aqueous 2-propanol (v/v), and vacuum dried

Conditions: temp:2.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A solution of 3-butyn-1-ol (365 g, 5.21 mol), triethylamine (526 g, 5.21 mol), and toluene (419 mL) was added to a cooled (0-5° C.) stirred solution of 4-chlorobenzenesulfonyl chloride (1.0 kg, 4.74 mol) and toluene (2.10 L). The reaction temperature was maintained below 20° C. during the addition. Precipitation of triethylamine hydrochloride salt occurred during the reaction. The reaction mixture was stirred at room temperature for 2-4 h. The triethylamine hydrochloride byproduct was separated by filtration and washed with toluene (2×350 mL). The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid. 2-Propanol (1.20 L) was added to the residue and the stirred solution was cooled to 20-25° C. Water (1.80 L) was added over 15 m. The slurry of product and solvent was cooled to 0-5° C. and stirred for 1 h. The white solid product was collected by filtration, washed with 33% aqueous 2-propanol (v/v), and vacuum dried to give 4-chloro-benzenesulfonic acid but-3-ynyl ester with 99% purity (as determined by HPLC. The reaction temperature was maintained below 20° C. during the addition Precipitation of triethylamine hydrochloride salt occurred during the reaction The triethylamine hydrochloride byproduct was separated by filtration washed with toluene (2×350 mL) The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid 2-Propanol (1.20 L) was added to the residue the stirred solution was cooled to 20-25° C Water (1.80 L) was added over 15 m The slurry of product and solvent was cooled to 0-5° C. stirred for 1 h The white solid product was collected by filtration washed with 33% aqueous 2-propanol (v/v), and vacuum dried

Conditions: temp:2.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A solution of 3-butyn-1-ol (365 g, 5.21 mol), triethylamine (526 g, 5.21 mol), and toluene (419 mL) was added to a cooled (0-5° C.) stirred solution of 4-chlorobenzenesulfonyl chloride (1.0 kg, 4.74 mol) and toluene (2.10 L). The reaction temperature was maintained below 20° C. during the addition. Precipitation of triethylamine hydrochloride salt occurred during the reaction. The reaction mixture was stirred at room temperature for 2-4 h. The triethylamine hydrochloride byproduct was separated by filtration and washed with toluene (2×350 mL). The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid. 2-Propanol (1.20 L) was added to the residue and the stirred solution was cooled to 20-25° C. Water (1.80 L) was added over 15 m. The slurry of product and solvent was cooled to 0-5° C. and stirred for 1 h. The white solid product was collected by filtration, washed with 33% aqueous 2-propanol (v/v), and vacuum dried to give 4-chloro-benzenesulfonic acid but-3-ynyl ester with 99% purity (as determined by HPLC. The reaction temperature was maintained below 20° C. during the addition Precipitation of triethylamine hydrochloride salt occurred during the reaction The triethylamine hydrochloride byproduct was separated by filtration washed with toluene (2×350 mL) The combined filtrates were concentrated to remove toluene under reduced pressure above 45° C. to maintain the residue as a liquid 2-Propanol (1.20 L) was added to the residue the stirred solution was cooled to 20-25° C Water (1.80 L) was added over 15 m The slurry of product and solvent was cooled to 0-5° C. stirred for 1 h The white solid product was collected by filtration washed with 33% aqueous 2-propanol (v/v), and vacuum dried