2,2-Dimethoxypropane → HCID 178450586, compound

In a 5 L round-bottom flask fitted with a thermometer, a nitrogen-introducing tube, and a stirrer were placed 1000 g of xylitol, 1916 g of 2,2-dimethoxypropane, and 37.5 mg of p-toluenesulfonic acid monohydrate and, with introduction of nitrogen thereinto, the reaction was carried out at 65° C. The solvent of the reaction solution was removed by distillation and purification by distillation (b.p. 108° C./0.15 mmHg) was performed to obtain an isomer mixture of 1,2,3,4-diisopropylidenexylitol (formula (5)) and 1,2,4,5-diisopropylidenexylitol (formula (6)). 1H-NMR (CDCl3, internal standard TMS) δ (ppm): 1.37-1.44 (12H, m, —C(CH3)2), 3.59-3.65 (1H, m, —CH—O—), 3.81-3.90 (2H, m, —CH2—O—), 3.98-4.01 (1H, m, —CH—O—), 4.04-4.10 (2H, m, —CH2—O—), 4.11-4.23 (1H, m, —CH—O—) 1H, m, —CH—O—)

1. customIn a 5 L round-bottom flask fitted with a thermometer
2. additiona nitrogen-introducing tube, and a stirrer
3. customwas carried out at 65° C
4. customThe solvent of the reaction solution was removed by distillation and purification by distillation (b.p. 108° C./0.15 mmHg)
5. customto obtain

ORD record

ord-68403d363515447283a15b7cc71a8c18

Source dataset

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08952125B2