HuagongsheHuagongshe Chemistry Print Report · For research reference only
Octanoyl chloride → HCID 20070872, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Octanoyl chloride | HCID 8124 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophen-3-ylmethyl-ammonium chloride | HCID 16956077 | — |
| Product | HCID 20070872 | HCID 20070872 | 89% |
Reaction Steps
Using the same reaction conditions as those of Example 4, 3-(aminomethyl)thiophene hydrochloride (4 mmol), triethylamine (4.4 mmol) and octanoyl chloride (40 mmol) were reacted to give N-(3-thienylmethyl)octanamide (0.85 g, 89%). M.p. 71°-72° C. (Found: C, 65.0; H, 8.4; N. 5.7; S, 13.2. Calculated for C13H21NOS: C, 65.3; H, 8.8; N, 5.9; S, 13.4%); EI m/e Intensity (%): 239 (19, M+), 97 (63, C4H3S.CH2+); δH(CDCl3) 7.03-7.33 (3H, m), 5.60 (1H, br,s), 4.44 (2H, d), 2.19 (2H, t), 1.61 (2H, m), 1.28 (8H, m), 0.87 (3H, t); δC(CDCl3): 14.2, 22.7, 25.8, 29.1, 29.3, 31.8, 36.9, 38.8, 122.3, 126.5, 127.1, 140.0, 173.1 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04992559 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-184bdaf819244518bfd8905af293c361 |
| Source note | uspto-grants-1991_02 |