Hydrochloric Acid → HCID 58681528, compound

Temperature

27.5 °C

To a suspension of L-cysteine (100 g) in ethanol (850 mL) under nitrogen was added over 40 min a solution of sodium hydroxide (2.0 eq., 64.6 g) in ethanol (650 mL) (the sodium hydroxide solution was maintained below 40° C. during its preparation, 3 hours for complete dissolution). After the addition, cyclopropylmethyl bromide (1.1 eq., 122.5 g) was added over 20 minutes while maintaining the temperature at 25-30° C. with a cold bath. The resulting white slurry was stirred for another 18 hours and then quenched by adding 2N HCl (0.73 eq., 300 mL) over 20 minutes. The thick suspension was concentrated (100 mbars, 52° C. bath) to about 400 mL (1.5L ethanol/water distilled) and then water (750 mL) was added. The pH (9.6) was adjusted to pH 6.5 with 2N HCl and the mixture was stirred at 4° C. for 2 hours and then filtered. The cake was washed five times with water (100 mL) and then dried in vacuum to afford S-cyclopropylmethyl-L-cysteine (128.2 g, 88.6% yield).

1. temperaturewas maintained below 40° C. during its preparation, 3 hours for complete dissolution)
2. additionwas added over 20 minutes
3. customquenched
4. concentrationThe thick suspension was concentrated (100 mbars, 52° C. bath)
5. distillationto about 400 mL (1.5L ethanol/water distilled)
6. additionwater (750 mL) was added
7. stirringthe mixture was stirred at 4° C. for 2 hours
8. filtrationfiltered
9. washThe cake was washed five times with water (100 mL)
10. customdried in vacuum

ORD record

ord-e14f409be3074c33bcb7c18f8570d381

Source dataset

uspto-grants-2005_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06977256B2