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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257218Generated: October 25, 2026

Dimethylformamide → HCID 14986508, compound

https://huagongshe.com/reaction/257218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-(Trifluoromethyl)benzamideHCID 74684—
ReactantPotassium BromideHCID 253877—
Reactant6-bromo-5,6-dihydro-7-hydroxy-5,5-dimethyl-7H-thieno[3,2-b]pyranHCID 14986486—
ProductHCID 14986508HCID 14986508—

Reaction Steps

The title compound was prepared as described in Example 3 starting with 6-bromo-7-hydroxy-5,6-dihydro-5,5-dimethyl-7H-thieno[3,2-b]pyran (4.5 g, 17.1 mmol) and 4-trifluoromethylbenzamide (7.43 g, 39.3 mmol) in N,N-dimethylformamide (75 mL) to give the product, 1.96 g (31%), as a colorless solid: mp 162°-163° C.; IR (KBr): 3396, 1664, 1534 and 1507 cm-1 ; MS: m/z 372 (MH+); 1H NMR (DMSO-d6): δ 1.21 (s, 3H), 1.40 {s, 3H), 3.80 (m, 1H, simplifies to d, J=8.7 Hz, with D2O), 5.01 (m, 1H, simplifies to d, J=8.7 Hz, with D2O), 5.68 (d, J=6.0 Hz, 1H, exchanges with D2O), 6.59 (d, J=5.7 Hz, 1H), 7.31 (d, J= 5.7 Hz, 1H), 7.88 (d, J=8.3 Hz, 2H), 8.11 (d, J=8.3 Hz, 2H) and 9.05 (d, J=8.4 Hz, 1H exchanges with D2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260453
Source datasetuspto-grants-1993_11
ORD IDord-660b96a3204a42aba86d70984ecb263e
Source noteuspto-grants-1993_11