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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638501Generated: October 30, 2026

Acetic Acid → HCID 86743498, compound

https://huagongshe.com/reaction/1638501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
Reactanttert-ButanolHCID 6386—
ReactantThymolHCID 6989—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 86743498HCID 8674349843%

Reaction Conditions

Temperature25 °C

Reaction Steps

Thymol (360.0 g, 2.4 mol) was added to a cooled (0° C.) mixture of acetic acid (600 mL) and sulfuric acid (144 mL). The mixture was allowed to warm to 20°-25° C., after which, t-butanol (228 mL, 2.4 mol) was added dropwise over a one hour period. The mixture was stirred at 25° C. for one hour. An additional portion of t-butanol (114 mL, 1.2 mol) was then added dropwise over a one hour period. The mixture was stirred at 25° C. for 4 hours after which the mixture was poured into hexane (1 L) and water (1 L) and the layers separated. The aqueous layer was extracted with hexane (2×100 mL). The combined extracts were washed with water (3×200 mL), saturated sodium bicarbonate solution (2×100 mL), water (200 mL) and brine (2×100 mL). The solvents were evaporated and the residue distilled to provide 262 g (bp 135°-145° C., 6 mm) of material which was crystallized from hexane to give 215.2 g (43% yield, GLC purity 99.5%) of 4-(1,1-dimethylethyl-2-(1-methylethyl)-5-methylphenol; mp 75.5°-76.5° C.; 1H-NMR (CDCl3)δ 1.24 (6H, d, J=7 Hz), 1.38 (9H, s), 2.42 (3H, s), 2.95-3.42 (1H, m), 4.67 (1H, broad s), 6.48 (1H, s), 7.13 (1H, s); IR (CHCl3)νmax 3575, 3340, 2940, 1605, 1670, 1490, 1450, 1400 cm-1 ; MS m/e 206, 191, 149, 121; UVλmax (ethanol) 223 nm (ε=5650), 253 nm (ε=2260).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880775
Source datasetuspto-grants-1989_11
ORD IDord-9742bd7a7c2d4a9d9d0d61478804b48a
Source noteuspto-grants-1989_11