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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596855Generated: November 2, 2026

Bisphenol A → HCID 131722863, compound

https://huagongshe.com/reaction/1596855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBisphenol AHCID 6623—
ReactantSodium HydroxideHCID 14798—
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant(+)-LimoneneHCID 440917—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
ProductHCID 131722863HCID 131722863—

Reaction Conditions

Temperature105 °C

Reaction Steps

A 250 ml flask with stir bar was charged with: 57 g of bisphenol-A (0.25 mole=0.50 equivalents) and 56 g (65 ml) of xylene. This was heated to 105° C. and there was then added 0.5 g of 50% triflic acid in water. Then 41 ml (34.4 g) d-limonene (99%) was added over 25 minutes at 105° C.±2° C. The reaction temperature was allowed to drop to 90° C. over 35 minutes at which time it was raised to 105° C. and an additional 40 ml of d-limonene (total of 68 g, 0.5 mols) was added over 45 minutes. After 1.5 hours at 105° C. catalyst was neutralized with 0.5 g of 15% sodium hydroxide in water. The well stirred reaction mixture was then allowed to stand overnite at room temperature. Then 176 g of liquor was separated from solid (salt), xylene, and unreacted d-limonene removed by vacuum distillation to 166° C. at 30 inches of vacuum. Yield of product and distillate was 111 g and 63 g respectively. Product was characterized by 3.8% free bisphenol-A; Mw/Mn of 310/235; and viscosity of 1250 cps (100° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291723B1
Source datasetuspto-grants-2001_09
ORD IDord-dbc64afa48d448d5b9f9f32b2bb0d8bf
Source noteuspto-grants-2001_09