Hydrochloric Acid → HCID 178501146, compound

Temperature

-50 °C

To a solution of dimethylsulfoxide (9.53 g, 122 mmol) in dry dichloromethane (400 ml) was slowly added oxalyl chloride (7.74 g, 61.0 mmol) at −78° C. The cooling bath was removed and the reaction mixture was stirred at −50° C. for 5 min. A solution of trans-4-hydroxymethyl-cyclohexanecarboxylic acid methyl ester (8.75 g, 50.8 mmol) in dichloromethane (108 ml) was added at −65° C. Stirring for 30 minutes was followed by addition of triethylamine (25.7 g, 254 mmol). The cooling bath was removed 15 minutes after completed addition. The reaction mixture was quenched with 1 M aqueous hydrochloric acid solution (152 ml, 152 mmol) at −10° C. The layers were separated. The organic layer was washed with two 250 ml-portions of water and one 100-ml portion of brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as yellow oil (9.3 g, quantitative), which was used in the next step without further purification. MS m/e: 170 (M+)

1. customat −78° C
2. customThe cooling bath was removed
3. stirringStirring for 30 minutes
4. customThe cooling bath was removed 15 minutes
5. additionaddition
6. customThe layers were separated
7. washThe organic layer was washed with two 250 ml-portions of water and one 100-ml portion of brine
8. dry with materialdried over anhydrous sodium sulfate
9. concentrationconcentrated in vacuo

ORD record

ord-79435c97d24749389e274427184c3df1

Source dataset

uspto-grants-2016_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09346824B2