تفاعل #80544

معادلة التفاعل

Na2CO3

(R)-8-fluoro-5-methoxy-3-[N-(4-methoxybenzylidene)-amino]-3,4-dihydro-2H-1-benzopyran

3 -Chloroperoxybenzoic acid

hydroxylamine hydrochloride

→

title compound

المردود 89.0%

(R)-8-Fluoro-3-hydroxylamino-5-methoxy-3,4-dihydro- 2H -1-benzopyran

المردود 89.0%

المذيبات

methanol

methylene chloride

Water

ظروف التفاعل

المعالجة

1. 1
   workup.STIRRINGThe mixture was stirred over night at room temperature
2. 2
   ترشيحPrecipitated 3-chlorobenzoic acid was filtered off
3. 3
   تركيزthe clear yellow filtrate was concentrated in vacuo
4. 4
   workup.STIRRINGthe resulting solution was stirred at room temperature for 2 h
5. 5
   أخرىThe solvent was evaporated
6. 6
   أخرىto give a thick orange oil
7. 7
   غسيلthe mixture was washed with ether (3×150 mL)
8. 8
   غسيلwashed with brine
9. 9
   تجفيفdried (Na2SO4)
10. 10
    ترشيحfiltered
11. 11
    تركيزconcentrated in vacuo
12. 12
    أخرىchromatographed on silica with EtOAc (15 to 50%) in hexane as eluent
13. 13
    أخرىchromatographed a second time on silica with EtOH- CHCl3 (1:99) as eluent

الإجراء التجريبي

3 -Chloroperoxybenzoic acid (85%; 7.6 g, 37.6 mmol) was added in portions to a stirred and cooled solution (+4° C.) of (R)-8-fluoro-5-methoxy-3-[N-(4-methoxybenzylidene)-amino]-3,4-dihydro-2H-1-benzopyran (10.8 g, 34 mmol) and methylene chloride (65 mL). The mixture was stirred over night at room temperature. Precipitated 3-chlorobenzoic acid was filtered off and the clear yellow filtrate was concentrated in vacuo. The oily residue was taken up in a solution of hydroxylamine hydrochloride (2.83 g, 40.8 mmol) and anhydrous methanol (60 mL) and the resulting solution was stirred at room temperature for 2 h. The solvent was evaporated to give a thick orange oil. Water was added to the oil, pH was adjusted to 8-9 with saturated aqueous Na2CO3 and the mixture was washed with ether (3×150 mL). The organic phases were combined, washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was flash chromatographed on silica with EtOAc (15 to 50%) in hexane as eluent. The resulting impure product was flash chromatographed a second time on silica with EtOH- CHCl3 (1:99) as eluent to give 6.45 g (89% yield) of the title compound as a colourless crystalline solid. Mp: 111°-113° C. [α]21D =+66.4° (C=1.3; CHCl3). GC-MS (70 eV) M=213 (56%).

المصدر