Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194914Generated: November 2, 2026

Hydrogen Bromide → HCID 88627039, compound

https://huagongshe.com/reaction/1194914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
ReactantHCID 140352840HCID 140352840—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
ProductHCID 88627039HCID 8862703923%

Reaction Steps

Ethyl (Z)-2-(tetrahydrothien-3-yloxyimino)-3-oxo-butyrate (1.29 g) was dissolved in a mixture of carbontetrachloride (15 ml), dichloromethane (5 ml) and methanol (2 ml). The mixture was cooled to -26°, a solution of hydrogen bromide in acetic acid (0.05 ml, 45% w/v) was added followed by bromine (0.29 ml). The mixture was allowed to warm to room temperature and stirred for 3 dyys. The solvents were removed under reduced pressure, the residue was partitioned between ethyl acetate and water. The organic layer was washed successively with saturated aqueous sodium bicarbonate, water and brine, then dried (MgSO4) and evaporated. Purification by flash chromatography with dichloromethane elution gave the title compound (0.4 g, 23%) as a pale yellow liquid. νmax (film) 2970, 2940, 1740, 1695, and 1600 cm-1. δH (CDCl3) 1.34 (3H, t), 2.04 (1H, m), 2.48 (1H, m), 2.90 (2H, m), 3.13 (2H, m), 4.33 (2H, s), 4.37 (2H, q), and 5.18 (1H, m). [Mass spectrum: +ve ion MH+ (324)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816452
Source datasetuspto-grants-1989_03
ORD IDord-55ed3f60085f4200849bff1612831fc2
Source noteuspto-grants-1989_03