HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379499Generated: October 31, 2026
Oxetane, 3,3-bis(chloromethyl)- → 1,4-Bis-[(3-chloromethyl-3-oxetanyl)methyloxy]butane
https://huagongshe.com/reaction/2379499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxetane, 3,3-bis(chloromethyl)- | HCID 6550 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Disodium | HCID 141233 | — |
| Product | 1,4-Bis-[(3-chloromethyl-3-oxetanyl)methyloxy]butane | HCID 53685635 | — |
Reaction Steps
Reaction of the disodium salt of butane 1,4-diol with excess 3,3-bis-(chloromethyl)oxetane gives 1,4-bis-[(3-chloromethyl-3-oxetanyl)methyloxy]butane (10). This difunctional oxetane can be further substituted to give multioxetane compounds having various pendant groups. Substitution of the difunctional oxetane can be tailored so that the multioxetane compound can react with oxetane monomers having widely varying reactivity ratios. Reaction of 1,4-bis-[(3-chloromethyl-3-oxetanyl)methyloxy]butane with sodium iodide gives 1,4-bis-[3-iodomethyl-3-oxetanyl)methyloxy]butane (11). Reaction of this diiodide with silver nitrate gives 1,4-bis-[(3-nitratomethyl-3-oxetanyl)methyloxy]butane (12), and with sodium azide it gives 1,4-bis-[(3-azidomethyl-3-oxetanyl)methyloxy]butane (13). ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05362848 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-ed380e02842f4d81bdd467f3618cf801 |
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| Source note | uspto-grants-1994_11 |
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