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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82439생성일: 2026년 10월 23일

Hydrochloric Acid → (3R,4S)-3-(benzyloxy)tetrahydro-2H-pyran-4-amine

https://huagongshe.com/ko/reaction/82439

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Pyridoxal 5'-phosphateHCID 1051—
반응물L-AlanineHCID 5950—
반응물Potassium CarbonateHCID 11430—
반응물Sodium Phosphate, DibasicHCID 24203—
반응물NadhHCID 439153—
반응물Sodium FormateHCID 2723810—
반응물(3S)-3-(benzyloxy)tetrahydro-4H-pyran-4-oneHCID 60209906—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물(3R,4S)-3-(benzyloxy)tetrahydro-2H-pyran-4-amineHCID 60209907—

반응 단계

To a solution of L-Alanine (200 g, 2.24 mol), sodium formate (76.0 g, 1.12 mmol), and sodium phosphate dibasic (28.7 g, 202 mmol) in 2.25 L of water adjusted to pH 7.5 was added NAD (2.2 g, 3.21 mmol), pyridoxal-5-phosphate (2.2 g, 8.90 mmol), LDH (0.45 g, 0.22 mol), FDH (4.5 g, 0.20 mol), and TA P1 G5 (4.5 g, 0.22 mol). After all the components were completely dissolved, (3S)-3-(benzyloxy)tetrahydro-4H-pyran-4-one (45 g, 0.22 mol) was added and the pH was adjusted to pH 7.25 with 6 N HCl and aged at 30° C. After 15 h, potassium carbonate (700 g, 5.06 mol) was added slowly, followed by ethyl acetate (2.2 L). The mixture was filtered through a bed of Solka Floc and the cake was washed with ethyl acetate (250 mL). The combined filtrates were separated and the aqueous layer was extracted a second time with ethyl acetate (2 L). The combined organic extracts were concentrated in vacuo to provide crude (3R,4S)-3-(benzyloxy)tetrahydro-2H-pyran-4-amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846702B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-07225e619eb640e285f6fccc978913dc
출처 메모uspto-grants-2014_09