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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420281Generated: November 1, 2026

Water → HCID 86735074, compound

https://huagongshe.com/reaction/2420281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AzideHCID 33557—
ReactantHCID 10910096HCID 10910096—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86735074HCID 86735074—

Reaction Steps

3,4-Epoxy-3,4-dihydro-2,2-dimethyl-2H-benzo[b]pyran (3.00g.) and sodium azide (1.23g.; an excess) were refluxed in dioxane (25 ml.) and water (5 ml.) mixture for 24 hours. Dilution with water and extraction via diethyl ether gave trans-4-azido-3,4-dihydro-2,2-dimethyl-2H-benzo[b]-pyran-3-ol (3.06 g.) as needles from 60°-80° petroleum ether m.p. 70°°- 71°. To a solution of the hydroxy azide (2.90g.) in acetone (50 ml.) containing concentrated hydrochloric acid (10 ml.) was added with stirring and in portions, zinc dust (10 g.). Stirring was continued until gas evolution ceased. The zinc was filtered and washed with acetone. The combined washings and filtrate were diluted with water and extracted with diethyl ether. Basification of the aqueous layer and isolation via diethyl ether gave trans-4-amino-3,4-dihydro-2,2-dimethyl-2H-benzo[b]pyran-3-ol (2.70 g.), re-crystallised from ethanol m.p. 138°. Treatment with anhydrous hydrochloric acid as in Example 1 yielded trans-4-amino-3,4-dihydro-2,2-dimethyl-2H-benzo[b]pyran-3-ol hydrochloride, m.p. 223°-225°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110347
Source datasetuspto-grants-1978_08
ORD IDord-ef43542f82084d8ab53e0b69c33d39ac
Source noteuspto-grants-1978_08