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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981781Generated: November 1, 2026

Octanoyl chloride → HCID 20070872, compound

https://huagongshe.com/reaction/981781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctanoyl chlorideHCID 8124—
ReactantTriethylamineHCID 8471—
ReactantThiophen-3-ylmethyl-ammonium chlorideHCID 16956077—
ProductHCID 20070872HCID 2007087289%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992559
Source datasetuspto-grants-1991_02
ORD IDord-184bdaf819244518bfd8905af293c361
Source noteuspto-grants-1991_02