Benzyl Alcohol → HCID 67440277, compound
Reaction equation
[NH2:1][C@@H:2]([CH2:6][CH:7]=[CH2:8])[C:3]([OH:5])=[O:4].S(Cl)([Cl:11])=O.C(OCC)C.O.[CH2:19](O)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[ClH:11].[NH2:1][C@@H:2]([CH2:6][CH:7]=[CH2:8])[C:3]([O:5][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:4]Participants
Procedure
To a solution of (2S)-2-amino-4-pentenoic acid 17 (225 mg, 1.96 mmol) in benzyl alcohol (5 mL) was added thionyl chloride (2 mL) and the resulting mixture was allowed to stir for 16 h before addition of diethyl ether (30 mL) and extraction with water (3×30 mL). The aqueous layer was concentrated, diluted with 2M sodium bicarbonate (20 mL), and extracted with DCM (3×30 mL). The combined organic fractions were dried and acidified with 1M HCl/diethyl ether (2 mL) and evaporated. The crude product dissolved in a minimal volume of MeOH and precipitated with diethyl ether to yield the title compound (322 mg, 1.34 mmol, 68%) as a white solid. [α]D20−40.6 (c. 0.1, H2O). Mp 186-191° C. 1H NMR (D2O, 300 MHz): δ 7.28 (m, 5H, ArH); 5.51 (m, 1H, H4); 5.11 (m, 4H, H5 and ArCH2); 4.08 (t, J=5.4 Hz, 1H, H2); 2.55 (m, 2H, H3). Mass Spectrum (CI, +ve) m/z 205 (25%) [MH+]. HRMS calcd for C12H16NO2 206.1181, found 206.1169.
Workup
- concentrationThe aqueous layer was concentrated
- additiondiluted with 2M sodium bicarbonate (20 mL)
- extractionextracted with DCM (3×30 mL)
- customThe combined organic fractions were dried
- customevaporated
- dissolutionThe crude product dissolved in a minimal volume of MeOH
- customprecipitated with diethyl ether
Sources & evidence
- ORD record
- ord-373c48794d8c49e3af0729114e0e647c
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08524657B2
Reaction notes
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