Hydrochloric Acid → HCID 86597003, compound
Reaction equation
Cl.[NH2:2][C@@H:3]([CH2:8][CH2:9][CH2:10][CH3:11])[C:4]([O:6][CH3:7])=[O:5].N1C=CC=CC=1.[C:18](Cl)(Cl)=[O:19].Cl>ClCCl.C1(C)C=CC=CC=1>[N:2]([C@@H:3]([CH2:8][CH2:9][CH2:10][CH3:11])[C:4]([O:6][CH3:7])=[O:5])=[C:18]=[O:19]Participants
Conditions
- Temperature
- 0 °C
Procedure
To 25.00 g (137.62 mmol) of methyl(2S)-2-aminohexanoate hydrochloride in 458 mL of dichloromethane at 0° C. was added 44.52 mL (550.49 mmol) of pyridine. Then, 85.57 mL (165.14 mmol) of a 1.93 M solution of phosgene in toluene was added to the solution and the mixture was stirred at 0° C. for 3 h. The solution was poured into 1N hydrochloric acid at 0° C. and extracted with dichloromethane. The organic layer was washed with 1N hydrochloric acid and saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated. The residue was purified by vacuum distillation at 80° C. @ 2 torr to give 21.32 g (91%) of methyl(2S)-2-isocyanatohexanoate. Rf=0.46 (1:4 ethyl acetate:hexanes); 1H NMR (300 MHz, DMSO-d6)δ 4.37 (dd, J=7 Hz, J=5 Hz, 1H), 3.73 (s, 3H), 1.78-1.60 (m, 2H), 1.36-1.16 (m, 4H), 0.85 (t, J=7 Hz, 3H); ES-MS m/z 172 (M+H).
Workup
- extractionextracted with dichloromethane
- washThe organic layer was washed with 1N hydrochloric acid and saturated sodium chloride
- dry with materialThe organic layer was dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- distillationThe residue was purified by vacuum distillation at 80° C. @ 2 torr
Sources & evidence
- ORD record
- ord-9e7916c3a4de4708944ed3bc6b39b6e1
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07282512B2
Reaction notes
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