HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254299Generated: November 2, 2026
Hydrochloric Acid → HCID 178508863, compound
https://huagongshe.com/reaction/2254299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 178507952 | HCID 178507952 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178508863 | HCID 178508863 | 79% |
Reaction Steps
A mixture of 136.7 g of bromoacetaldehyde diethylacetal, 347 mL of water, and 17.3 mL of concentrated HCl was heated to about 90° C. with vigorous stirring for about 30 minutes, at which time a clear solution was obtained. The solution was cooled to room temperature and 68.3 g of NaOAc was added. The resulting solution was added, with stirring, to a suspension of 100 g of 2,4-diamino-6-hydroxypyrimidine and 34.2 g of NaOAc in 739 mL of water, which had been heated to 70°-85° C. The reaction was allowed to proceed for 2 hours at 70°-85° C., at which time the reaction was complete. The mixture was cooled to 0° C. and held for about 1.5 hours. The mixture was then filtered and the collected product was washed with 500 mL of water and 500 mL of acetone, and dried, affording 72.3 g (79%) of 2-amino-4-hydroxypyrrolo[2,3-d]pyrimidine. A small sample was further purified by slurry in hot methanol, filtration, and drying, mp>300° C. 1H NMR (300 MHz, DMSO-d6) δ6.03 (s, 2 H), 6.13 (m, 1 H), 6.56 (dd, J=3.3, 2.3 Hz, 1 H), 10.23 (bs, 1 H), 10.93 (bs, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05235053 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-a3b08a8e97f94beabd66df4100d8afb8 |
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| Source note | uspto-grants-1993_08 |
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