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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420321Generated: October 28, 2026

3-tert-butylbenzaldehyde → HCID 66649701, compound

https://huagongshe.com/reaction/420321

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-tert-butylbenzaldehydeHCID 10192588—
ReactantHCID 86639544HCID 86639544—
ProductHCID 66649701HCID 66649701—

Reaction Steps

The title compound was prepared in an analogous manner as described for example 1h, starting from (1S,3R,4S,5S)-3-amino-5-[3-fluoro-4-nitro-5-((R)-2,2,2-trifluoro-1-methoxy-methyl-ethoxy)-benzyl]-1-oxo-tetrahydro-thiopyran-4-ol TFA salt (310 mg, 0.7 mmol) and 3-tert-butyl-benzaldehyde and was obtained after purification by flash-chromatography (hexane-(EtOAc-MeOH 9:1) gradient) as a light yellow foam: TLC (EtOAc-MeOH 9:1) Rf=0.38; HPLC RtH1=1.05 min; ESIMS [M+H]+=591; 1H NMR (600 MHz, CDCl3): δ 7.36 (s, 1H), 7.28 (s, 1H), 7.23 (m, 2H), 7.13 (d, 1H), 7.11 (d, 1H), 5.66 (m, 1H), 5.16 (d, 1H), 3.83-3.79 (m, 2H), 3.69 (dd, 1H), 3.63 (d, 1H), 3.55 (m, 1H), 3.30 (s, 3H), 3.14 (m, 2H), 3.00 (d, 1H), 2.55 (m, 1H), 2.5-2.4 (m, 3H), 1.95 (m, 1H), 1.25 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-126fd33d37c24166a086f0b9144974b6
Source noteuspto-grants-2012_01