HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085534Generated: October 25, 2026
Carbon tetrabromide → 5'-Azido-2',5'-dideoxy-5-(2-chloroethyl)uridine
https://huagongshe.com/reaction/1085534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Lithium azide | HCID 88163 | — |
| Reactant | 5-(2-Chloroethyl)-2'-deoxyuridine | HCID 514814 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5'-Azido-2',5'-dideoxy-5-(2-chloroethyl)uridine | HCID 54002307 | 31.6% |
Reaction Steps
1.4 g of 5-(2-chloroethyl)-2'-deoxyuridine and 1.3 g of triphenylphosphine were dissolved in 20 ml of dimethylformamide and stirred while 1.2 g of lithium azide were added to give a solution within 5 minutes at room temperature. 1.7 g of carbon tetrabromide were added portionwise during 5 minutes to give a hazy orange colored solution which was stirred at room temperature for 17 hours. 5 ml of methanol were added to give a clear solution. After 0.5 hour, the solvents were removed by evaporation under an oil pump vacuum to give a gum which was partitioned between 30 ml of ethyl acetate and 20 ml of water. The white solid which formed was removed by filtration to give 0.64 g of crude product of melting point 179°-182° C. (decomposition). This crude product was stirred with methanol and then removed by filtration to give 0.48 g of pure 5'-azido-2',5'-dideoxy- 5-(2-chloroethyl)-uridine of melting point 197°-199° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05010060 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-4ca87d5efd4d46d5bbe506021ac72059 |
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| Source note | uspto-grants-1991_04 |
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