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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086639Generated: October 30, 2026

Acetic Anhydride → HCID 67887508, compound

https://huagongshe.com/reaction/1086639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium BromideHCID 253877—
Reactant5,6-Dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyranHCID 9903464—
CatalystPerchloric AcidHCID 24247—
ProductHCID 67887508HCID 67887508—

Reaction Steps

A solution of 5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyran (2.0 g, 7.48 mmol) and perchloric acid (70%, 10 drops) in acetic anhydride (20 mL) were stirred for 1 h at 0°-5° C. The solution was poured into ice water (100 mL). The product was extracted into dichloromethane, washed with water (4×), and evaporated in vacuo. The resultant oil was purified by flash chromatography, using 1% methanol in dichloromethane as the eluant, then crystallized from hexanes to give the product, 2.12 g (92%), as a colorless solid: mp 92°-93° C.; IR (KBr): 1745 and 1684 cm-1 ; MS: 310 (MH+); 1H NMR (CDCl3): δ1.37(s, 3H), 1.38(s, 3H), 1.98(m, 2H), 2.10(s, 3H), 2.37(m, 2H), 3.24(m, 1 H), 3.40(m, 1H), 5.15(d, J=9.1 Hz, 1H), 5.44(d, J=9.1 Hz, 1H), 6.58(d, J=5.4 Hz, 1H) and 7.13(d, J=5.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030736
Source datasetuspto-grants-1991_07
ORD IDord-afa3ca739d334fe5b5973616203b44e9
Source noteuspto-grants-1991_07