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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1110190생성일: 2026년 10월 26일

Sulfuric Acid → Fmoc-Asn(Trt)-OH

https://huagongshe.com/reaction/1110190

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물TriphenylcarbinolHCID 6457—
반응물Acetic AnhydrideHCID 7918—
반응물FMOC-L-asparagineHCID 2724774—
용매Acetic AcidHCID 176—
생성물Fmoc-Asn(Trt)-OHHCID 640248—

반응 단계

A suspension of 3.54 g of Fmoc-Asn-OH (10 mmol) and 5.2 g of triphenylmethanol (20 mmol) in 30 ml of acetic acid and 1.9 ml of acetic anhydride (20 mmol) is stirred at 50° for 15 minutes and then a solution of 0.05 ml of conc. sulfuric acid in 5 ml of acetic acid is added. After about one hour at 50° C. a solution forms, and after 11/2 hours a precipitate starts to form. After 3 hours, 200 ml of ice-cold water are slowly added to the suspension, while cooling in ice, the mixture is briefly stirred, and the precipitate is filtered off and thoroughly washed with water. The moist material is dissolved in ethyl acetate, and the organic phase is washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. Before the product starts to crystallize out, the solution is diluted with 1,2-dichloroethane, concentrated again and filtered through 50 g of silica gel. The excess triphenylmethanol is eluted with 200 ml of 1,2-dichloroethane, and then Fmoc-Asn(Trt)-OH is eluted with 500 ml each of a 98:2 and of a 96:4 mixture, of 1,2-dichloroethane and methanol. The residue after evaporation to dryness is dissolved in 10 ml of tetrahydrofuran, 30 ml of ethyl acetate are added, the solution is concentrated to 20 g, and diisopropyl ether is added to crystallize; the Fmoc-Asn(Trt)-OH obtainable in this way melts at 210°-211° (with decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05324833
출처 데이터셋uspto-grants-1994_06
ORD IDord-7cef292f1ecc4446bad86c1b852f9879
출처 메모uspto-grants-1994_06