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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285015Generated: October 30, 2026

HCID 13587575, compound → HCID 20251456, compound

https://huagongshe.com/reaction/1285015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13587575HCID 13587575—
SolventEthanolHCID 702—
ProductHCID 20251456HCID 2025145695.3%

Reaction Steps

To a mixture of 40 grams of 1-butyl 3,4,4,6-tetramethyl 1,2,3,4-tetrahydropyrimidine prepared as described in example 7, and 177 grams of absolute ethanol was added over a 1/2 hour period 4.7 grams of sodium hydridoborate. The reaction mixture was stirred for 18 hours and the ethanol evaporated under diminished pressure. To the resulting product was added water and stirring was continued for 24 hours. The organic layer was separated, dissolved in ether, and the ethereal solution washed with diminished pressure to yield 38.5 grams of 1-butyl 3,4,4,6-tetramethyl hexahydropyrimidine. C13 n.m.r., solvent CDCl3 ; ref. T.M.S.; ##STR13## 71.2(2); 52.4(4); 46.4(5); 52.1(6); 29.7(7); 20.4(8); 15.3(9); 34.7(10); 49.6(11); 29.5(12); 20.9(13); 14.0(14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564707
Source datasetuspto-grants-1986_01
ORD IDord-d83df170e8bb4e4c88ebcb2917768e75
Source noteuspto-grants-1986_01