Hydrochloric Acid → 3-Carboxytyrosine

A 250 mL 3-necked flask equipped with a magnetic stirrer and a condenser was charged with 4.1 g of 3-cyano-L-tyrosine and 100 mL of 6N aqueous HCl. The mixture was heated to reflux with stirring. After 36 h, HPLC (C18, 90:10:0.1 H2O:MeCN:TFA) indicated no remaining starting material at k′=1.33 and a major new component at k′=1.69. The reaction mixture was cooled to RT, filtered to remove solids, and concentrated in vacuo to dryness. The residue was dissolved in 100 mL of 8:2 H2O:MeOH and the solution was passed through two C18 plugs (3.5×4.5 cm, EM separations LiChroprep RP-18) washing with 8:2 H2O:MeOH. The filtrate was concentrated in vacuo to dryness to afford 4.5 g of 3-carboxytyrosine as a brown solid. A portion of this material (1.30 g) was dissolved in 40 mL of 1,4dioxane with 2 mL of concentrated H2SO4 and the solution was added to 30 mL of isobutylene (condensed at −78° C.) in a 300 mL pressure bottle equipped with a magnetic stirrer. The vessel was stoppered, warmed to RT and stirred. After 48 h, the bottle was cooled to 0° C. in an ice water bath, opened, and the mixture was treated with 20 g of NaHCO3. After allowing the isobutylene to evaporate, the mixture was suspended in 300 mL of water and extracted with CH2Cl2 (4×100 mL). The combined CH2Cl2 extracts were washed with 5% aqueous NaHCO3 (2×50 mL), dried over anhydrous MgSO4, and concentrated in vacuo to give a yellow-brown oil. Analysis by tlc (SiO2, 97:3 CH2Cl2:MeOH) indicated a major component at Rf=0.41 and three minor components at Rf=0.30, 0.25 and 0.0. The crude material was purified by flash chromatography on 75 g of silica gel (94:6 CH2Cl2:MeOH) to give 1.2 g of a light yellow oil. The oil was dissolved in 40 mL of ether and treated with 3.9 mL of 1M ethereal HCl. A precipitate formed which was collected by filtration and dried in vacuo to afford 1.14 g (53%) of tert-butyl 3-(tert-butoxycarbonyl)-L-tyrosinate HCl as a fluffy white solid. An analytical sample (26 mg) was prepared by recrystallization from MeOH-ether, m.p. 205° C. (dec).

1. customA 250 mL 3-necked flask equipped with a magnetic stirrer and a condenser
2. temperatureThe mixture was heated
3. temperatureto reflux
4. filtrationfiltered
5. customto remove solids
6. concentrationconcentrated in vacuo to dryness
7. dissolutionThe residue was dissolved in 100 mL of 8:2 H2O
8. washwashing with 8:2 H2O
9. concentrationThe filtrate was concentrated in vacuo to dryness

ORD record

ord-6c4c059da755407d8a5ed5a0663bbe7b

Source dataset

uspto-grants-2001_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06319702B1