Thionyl Chloride → HCID 14580383, compound
Reaction equation
[N:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9]([OH:11])=O)=[N+:2]=[N-:3].S(Cl)([Cl:14])=O>>[N:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9]([Cl:14])=[O:11])=[N+:2]=[N-:3]Participants
3
Procedure
The above compound was prepared by a literature procedure [V. M. Rothe and K. Gehrke, Makromol Chem. 83, 1 (1965)] as follows: To 6-azidohexanoic acid (7.5 g, 47.7 mmol) previously cooled to 0° C. was added 10 ml (16.3 g, 137 mmol) of thionyl chloride and the solution was stirred in cold until the evolution of gas had subsided (5-10 min) and then refluxed for 1 h. The reaction mixture was evaporated and the residue distilled to give 5.5 g (65.6%) of title compound bp 110°-111° C./12 Tor (lit. bp 73°-75° C./0.1 torr); ir (neat) νmax : 2097 (N3), 1795 cm-1 (C=O); 1Hmr (CDCl3) δ: 1.1-2.0 (m, 6H, 3CH2), 2.9 (m, 2H, CH2CO), 3.27 (m, 2H, CH2N 3).
Workup
- customThe above compound was prepared by a literature procedure [V. M. Rothe and K. Gehrke, Makromol Chem. 83, 1 (1965)]
- custom(5-10 min)
- temperaturerefluxed for 1 h
- customThe reaction mixture was evaporated
- distillationthe residue distilled
Sources & evidence
- ORD record
- ord-9642e2d5bd604a5ba19a36594c8fb2dc
- Source dataset
- uspto-grants-1983_03
- Patent number
- US04378314
Reaction notes
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