Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254299Generated: November 2, 2026

Hydrochloric Acid → HCID 178508863, compound

https://huagongshe.com/reaction/2254299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodium AcetateHCID 517045—
ReactantHCID 178507952HCID 178507952—
SolventWaterHCID 962—
ProductHCID 178508863HCID 17850886379%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05235053
Source datasetuspto-grants-1993_08
ORD IDord-a3b08a8e97f94beabd66df4100d8afb8
Source noteuspto-grants-1993_08