反应详情

温度

25 °C

4-Aminomethylbenzoic acid methyl ester hydrochloride (1.45 g, 7.2 mmol) was suspended in 1,2-dichloroethane (50 mL) and added saturated aqueous potassium carbonate. The phases were separated and the aqueous layer was extracted with another portion of 1,2-dichloroethane (50 mL). The combined organic phases were added glacial acetic acid (435 μL, 7.6 mmol) followed by spiro[5.5]undecan-3-one (1.2 g, 7.2 mmol). The suspension was stirred for 30 min at 25° C. and sodium triacetoxyborohydride (2.27 g, 10.7 μmol) was added. After stirring for 2 days at 25° C., water (100 mL) and saturated aqueous potassium carbonate (15 mL) were added. The phases were separated and the aqueous layer was extracted with 1,2-dichloroethane (2×100 mL). The combined organic phases were washed with water (100 mL) and brine (100 mL), dried over MgSO4 and evaporated to afford 4-(spiro[5.5]undec-3-ylaminomethyl)benzoic acid methyl ester which was used in the subsequent steps without further purification.

1. customThe phases were separated
2. extractionthe aqueous layer was extracted with another portion of 1,2-dichloroethane (50 mL)
3. stirringAfter stirring for 2 days at 25° C.
4. customThe phases were separated
5. extractionthe aqueous layer was extracted with 1,2-dichloroethane (2×100 mL)
6. washThe combined organic phases were washed with water (100 mL) and brine (100 mL)
7. dry with materialdried over MgSO4
8. customevaporated