Glycine → N-[(4-Bromophenyl)methyl]glycine

i)—To a solution of glycine (15 g, 200 mmol) in water (80 ml) were added an aqueous solution of sodium hydroxide (20 ml, 10 M) and a solution of 4-bromobenzaldehyde (37 g, 200 mmol) in methanol (440 ml). After 10 minutes stirring at room temperature sodium borohydride (7.5 g, 200 mmol) was added in portions to this suspension. After 18 h stirring at room temperature the reaction mixture was concentrated under reduced pressure and washed with diethyl ether. The aqueous phase was neutralized with concentrated hydrochloric acid. The precipitate was collected by filtration, washed with water and diethyl ether. Drying the white solid afforded 2-(4-bromobenzylamino)acetic acid (14.98 g). The product was used in the following step without purification.

1. additionwas added in portions to this suspension
2. concentrationwas concentrated under reduced pressure
3. washwashed with diethyl ether
4. filtrationThe precipitate was collected by filtration
5. washwashed with water and diethyl ether
6. customDrying the white solid

ORD record

ord-eb2eb18f8b8949b0bbff36403de82c57

Source dataset

uspto-grants-2011_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07960560B2