HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052195Generated: November 4, 2026
Hexamethylenetetramine → HCID 20337667, compound
https://huagongshe.com/reaction/2052195
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2-Bromo-1-[4-(tetradecyloxy)phenyl]ethan-1-one | HCID 53994698 | — |
| Product | HCID 20337667 | HCID 20337667 | 95% |
Reaction Steps
88 g of p-tetradecyloxy-ω-bromoacetophenone are dissolved in 320 ml of anhydrous chloroform. 30.4 g of urotropine are added at room temperature. The solution heats up spontaneously. It is then stirred for 2 hours at room temperature. The chloroform is evaporated off and the solid residue is triturated with acetone. The crystalline precipitate is suction filtered and washed several times with acetone. The crude product is then introduced into a solution of 140 ml of concentrated hydrochloric acid in 1000 ml of ethanol and stirred for 24 hours at room temperature. The product is suction filtered and washed with a mixture of ethanol and concentrated hydrochloric acid (7:1). 80 g =95% of p-tetradecyloxy-ω-aminoacetophenone-hydrochloride melting at 190° to 195° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04183752 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-26dcca492c964e50af4a71761917c409 |
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| Source note | uspto-grants-1980_01 |
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