Water → 2,5-Dichloro-4-pyrrolidin-1-ylmethyl-phenol

Pyrrolidine (0.48 mL, 5.76 mmol) was added to a suspension of Intermediate 24, 2,5-Dichloro-4-hydroxybenzaldehyde (0.88 g, 4.6 mmol) in dichloromethane (10 mL). The reaction mixture was cooled with an ice bath. Sodium triacetoxyborohydride (1.22 g, 5.76 mmol) was added in portions under stirring. The reaction mixture was stirred for 12 h at room temperature. Water (20 mL) and dichloromethane (10 mL) were added. The reaction mixture was acidified with 5N NAHSO4 to pH˜2. The organic layer was separated. The aqueous one was subjected to extraction with CH2Cl2 (2×30 mL), and the extracts were discarded. The aqueous fraction was alkalized with a saturated solution of potassium carbonate to pH 9-10. The product was extracted with CH2Cl2 (3×20 mL). The organic layer was dried with anhydrous Na2SO4 (5 g). The solvent was evaporated in vacuo, and coevaporated with dioxane to give the title compound (0.89 g, 3.6 mmol, 79%) as pale-yellow crystals. LC/MS data: 248.0, 247.0 and 246.0 (M+H); 174.9 (M-pyrrolidine+H) (calculated for C11H13ClNO 246.1). 1H NMR data (DMSO-d6): 10.52 (br.s., 1H, OH); 7.38 (s, 1H, s Ar—H); 6.98 (s, 1H, Ar—H); 3.54 (s, 2H, CH2Ar); 2.40-2.47 (m, 4H); 1.63-1.74 (m, 4H).

1. temperatureThe reaction mixture was cooled with an ice bath
2. stirringThe reaction mixture was stirred for 12 h at room temperature
3. customThe organic layer was separated
4. extractionThe aqueous one was subjected to extraction with CH2Cl2 (2×30 mL)
5. extractionThe product was extracted with CH2Cl2 (3×20 mL)
6. dry with materialThe organic layer was dried with anhydrous Na2SO4 (5 g)
7. customThe solvent was evaporated in vacuo

ORD record

ord-8395a4e2972f4607bf9e9a502b399f1d

Source dataset

uspto-grants-2010_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07812040B2