Water → N-t-butoxycarbonyl-p-hydroxymethylphenylglycine

To a solution of p-hydroxymethylphenylglycine (8.0 g., 0.044 mole) and triethylamine (8.8 g., 0.087 mole) in 160 ml. water was added t-butoxycarbonyl azide (6.95 g., 0.049 mole) dissolved in 120 ml. tetrahydrofuran. After stirring overnight at room temperature, the reaction mixture was washed twice with 200 ml. portions of ether. The aqueous layer was covered with ether and in an ice bath was acidified to pH 3-3.5 with 3 N hydrochloric acid. The acidic solution was extracted three times with 200 ml. portions of ether. The combined ether layers were washed with saturated sodium chloride solution, dried, and the ether evaporated under reduced pressure. The resulting oil was triturated with chloroform-hexane and the solid filtered off to give dl-N-t-butoxycarbonyl-p-hydroxymethylphenylglycine (7.74 g., 63% yield), m.p. 139°-141.5° (dec.).

1. dissolutiondissolved in 120 ml
2. washthe reaction mixture was washed twice with 200 ml
3. customThe aqueous layer was covered with ether and in an ice bath
4. extractionThe acidic solution was extracted three times with 200 ml
5. washThe combined ether layers were washed with saturated sodium chloride solution
6. customdried
7. customthe ether evaporated under reduced pressure
8. customThe resulting oil was triturated with chloroform-hexane
9. filtrationthe solid filtered off

ORDレコード

ord-6f890e6b0c7445a0836168b3a244d326

出典データセット

uspto-grants-1981_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04297489