Hydrochloric Acid → HCID 10858216, compound

Temperature

-20 °C

Triethylamine (100 mL, 0.72 mol) was added to a solution of (R)-2-methylbutane-1,4-diol (30 g, 0.29 mol) in DCM (600 mL). The solution was cooled to −20° C., and methanesulfonyl chloride (49 mL, 0.63 mol) was added dropwise over 30 min with vigorous stirring. The resulting mixture was stirred for additional 1 h while the temperature was maintained between −20 and −15° C. The mixture was allowed to warm to 0° C. and then poured into cold 1N HCl solution (100 mL). The organic layer was separated and aqueous phase was extracted with DCM (100 mL). The combined organic extracts were washed with saturated aqueous NaHCO3 solution, brine, dried over MgSO4, filtered, and concentrated in vacuo. The resulting product (75.9 g, quant) was used directly for the next step. 1H NMR (400 MHz, CDCl3): δ 4.41-4.24 (m, 2H), 4.12 (dq, 2H), 3.02 (d, 6H), 2.13 (td, 1H), 1.95 (td, 1H), 1.80-1.65 (m, 1H), 1.07 (d, 3H).

1. temperaturewas maintained between −20 and −15° C
2. temperatureto warm to 0° C.
3. customThe organic layer was separated
4. extractionaqueous phase was extracted with DCM (100 mL)
5. washThe combined organic extracts were washed with saturated aqueous NaHCO3 solution, brine
6. dry with materialdried over MgSO4
7. filtrationfiltered
8. concentrationconcentrated in vacuo

ORD record

ord-a1144691e41d43b3a2f7df6b55a6dac8

Source dataset

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09187460B2