HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280732Generated: October 25, 2026
1,4-Dibromo-2,2-diethoxy-3-butanone → HCID 178467676, compound
https://huagongshe.com/reaction/280732
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dibromo-2,2-diethoxy-3-butanone | HCID 13100973 | — |
| Reactant | HCID 178513045 | HCID 178513045 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methane | HCID 297 | — |
| Product | HCID 178467676 | HCID 178467676 | 71.9% |
Reaction Steps
A mixture of 25.5 g (80 mmol) of 1,4-dibromo-2,2-diethoxy-3-butanone, 11.8 g (100 mmol) of N-amidinothiourea, and 150 ml of tetrahydrofuran was heated at reflux for 3 hours. The mixture was filtered to remove some insoluble solid, and the filtrate was concentrated. The residue was triturated with 200 ml of saturated sodium bicarbonate, then extracted four times with a total of 500 ml of ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulfate, filtered and evaporated leaving a solid. Recrystallization from 250 ml of acetonitrile, after decolorization with charcoal, afforded 9.7 g (36%) of 2-guanidino-4-(2-bromo-1,1-diethoxyethyl)thiazole as a white solid, mp 157°-158°; calcd. for C10H17N4O2SBr: C, 35.62; H, 5.08; N, 16.61; Br, 23.69; S, 9.51; found: C, 35.60; H, 4.97; N, 16.99; Br, 23.75; S, 9.59.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590299 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-f3ffcaeabb7f4ad9ac8cf42c953eed67 |
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| Source note | uspto-grants-1986_05 |
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