참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 4-Nitro-3-phenyl-L-alanine | HCID 13706 | — |
| 생성물 | Methyl p-nitrophenylalanine hydrochloride | HCID 69555327 | — |
반응 단계
Dry methanol (200 ml) was saturated with HCl(g) in a two-necked round bottom flask cooled to -10° C. p-Nitrophenylalanine (10.0 g, 47.6 mmol) was added in one portion and left to stir for about 18 hours, the solution was evaporated to near dryness on a rotary evaporator and the precipitated product collected in a Buchner funnel. After drying under vacuum at about 50° C., the yield was 10.97 grams (88.3%). A TLC (thin layer chromatography) of the free amino ester run in CHCl3 :MeOH (4:1) revealed and Rf =0.85-0.88. 1H NMR (220 MHz, D2O, pH 1.5) 8.20 (d,2 J=10.0), 7.53 (d,2,J=10.0), 4.55 (t,1,J=5.00), 3.84 (s,3), 3.43 (m,2); CI-MS 225 ((M+1)/z). Anal. Calcd. for C10H13N2O4Cl: C, 46.07; H, 5.03; N, 10.74; Cl, 13.60. Found: C, 45.87; H, 5.08; N, 10.48; Cl, 13.58.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05246692 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-07d855b37c5b4d328abc877c7bed7d1e |
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| 출처 메모 | uspto-grants-1993_09 |
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