Sulfuric Acid → (1R,2S)-(+)-cis-1-Amino-2-indanol

Into a 10 ml eggplant-type flask, 1.07 g (5.0 mmol) of trans-(-)-2-bromo-1-indanol (I: X=OH, Y=Br; optical purity based on specific rotation: 42.5%) and 2.6 ml of acetonitrile were introduced. While this mixture was stirred with a magnetic stirrer, 0.76 g (7.5 mmol) of 97% sulfuric acid was dropwise added thereto in a period of 2 hours at room temperature. The resulting mixture was stirred at room temperature for 1 hour and then 6.5 ml of water was added thereto. After an acetonitrile/water azeotrope was distilled off under a reduced pressure of 200 mmHg at 40° C., the remaining mixture was stirred for 4.5 hours at 60° C. This reaction liquid was cooled to room temperature and then washed twice with 10 ml of dichloromethane. An aqueous solution of 25% sodium hydroxide was added to the water phase to attain a pH of 7. The resulting solution was washed twice with 10 ml of dichloromethane. Then, the pH of the water phase was adjusted to 11 by an addition of an aqueous solution of 25% sodium hydroxide. This phase was extracted with 10 ml of dichloromethane three times. The extracted phase was dried with sodium sulfate anhydride and then evaporated to dryness in vacuo to yield 0.47 g of cis-(+)-1-aminoindan-2-ol (V) as a white crystal (yield: 63.0%). According to an HPLC, its chemical purity and optical purity based on specific rotation were 98.8% and 42.0%, respectively.

1. stirringThe resulting mixture was stirred at room temperature for 1 hour
2. distillationAfter an acetonitrile/water azeotrope was distilled off under a reduced pressure of 200 mmHg at 40° C.
3. stirringthe remaining mixture was stirred for 4.5 hours at 60° C
4. customThis reaction liquid
5. washwashed twice with 10 ml of dichloromethane
6. additionAn aqueous solution of 25% sodium hydroxide was added to the water phase
7. washThe resulting solution was washed twice with 10 ml of dichloromethane
8. additionThen, the pH of the water phase was adjusted to 11 by an addition of an aqueous solution of 25% sodium hydroxide
9. extractionThis phase was extracted with 10 ml of dichloromethane three times
10. dry with materialThe extracted phase was dried with sodium sulfate anhydride
11. customevaporated to dryness in vacuo

ORD 기록

ord-bd17f0cd008e4ee1ba05d2236df355a1

출처 데이터셋

uspto-grants-1997_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05648534