HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638733Generated: October 30, 2026
1,4-Dioxane → Ethane-1,2-diyl bis(2-(4-isocyanatophenoxy)acetate)
https://huagongshe.com/reaction/638733
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | (4-Amino-phenoxy)-acetic acid-2-[2-(4-amino-phenoxy)-acetoxy]-ethyl ester | HCID 25235089 | — |
| Product | Ethane-1,2-diyl bis(2-(4-isocyanatophenoxy)acetate) | HCID 49764366 | 44.2% |
Reaction Steps
(4-Aminophenoxy)acetic acid 2-[2-(4-aminophenoxy)acetoxy]ethyl ester 43 (5 g, 14.3 mmol) was dissolved in dry dioxane (80 ml) under nitrogen atm. and cooled to below 20° C. A solution of triphosgene (7 g, 23.6 mmol) in dry dioxane (20 ml) was added drop wise. The mixture was heated slowly to 75-80° C. and maintained for 2½ hours. The condenser was then arranged for distillation and solvent removed by distillation at atmospheric pressure until the volume of the reaction mixture was reduced to approximately one third. Fresh dry dioxane (50 ml) was added and the solvents were distilled off under vacuum. The residue was re-evaporated two times from dry dioxane to give crude 44. Crude 44 was recrystallised from a mixture of toluene:hexane (1:3) to give pure 44 (2.6 g, 44.2%) as a white powder. M.p: 96-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691364B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-c6bf707526ba408ab9ba4b697922f0a2 |
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| Source note | uspto-grants-2010_04 |
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