تفاعل #1269901

معادلة التفاعل

1-benzyl-4-piperidone

2-bromo-5-fluorobenzoic acid

n-butyllithium

hexane

→

1′-benzyl-5-fluoro-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one

المردود 33.3%

المذيبات

ether

water

tetrahydrofuran

tetrahydrofuran

ظروف التفاعل

المعالجة

1. 1
   استخلاصThe aqueous layer was extracted with ether (2×40 ml)
2. 2
   workup.WAITboiled for 1 hour
3. 3
   درجة الحرارةThe mixture was cooled to 0° C.
4. 4
   استخلاصrapidly extracted with dichloromethane (3×80 ml)
5. 5
   غسيلThe combined extracts were washed with water (80 ml)
6. 6
   تجفيفdried over Na2SO4
7. 7
   ترشيحfiltered
8. 8
   تركيزconcentrated in vacuo
9. 9
   أخرىThe crude oil was chromatographed on silica gel (eluent: heptane/ethylacetate 1:1)

الإجراء التجريبي

To a stirred solution of 2-bromo-5-fluorobenzoic acid (5.0 g, 21.9 mmol) at −70° C. in tetrahydrofuran (30 ml) was added dropwise a 1.6M n-butyllithium solution in hexane (44 ml, 70.1 mmol) over a period of 1 hour. After 3 hours, a solution of 1-benzyl-4-piperidone (8.5 g, 43.8 mmol) in tetrahydrofuran (20 ml) was added dropwise. The mixture was allowed to warm to room temperature and stirred overnight. The mixture was poured into a stirred mixture of water (150 ml) and ether (150 ml). The aqueous layer was extracted with ether (2×40 ml), acidified with HCl 5 N (20 ml) to pH 2 and boiled for 1 hour. The mixture was cooled to 0° C., basified (pH 10) with NaOH 5 N and rapidly extracted with dichloromethane (3×80 ml). The combined extracts were washed with water (80 ml), dried over Na2SO4, filtered and concentrated in vacuo. The crude oil was chromatographed on silica gel (eluent: heptane/ethylacetate 1:1) to yield 2.27 g (33%) of 1′-benzyl-5-fluoro-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one as light yellow solid. MS m/e: 312 (M+H+).

المصدر